375 recalls are still open: 363 from FDA and 12 from USDA, plus 100 USDA public health alerts. USDA has named 546 stores for its open recalls.
Everything here is in the agencies’ own words. FDA data: enforcement reports marked “Ongoing” (FDA updates them weekly; as of Sep 30, 2026). USDA data: recalls marked “Active” on fsis.usda.gov (checked Oct 09, 2026). Groups are sorted by the reason the agency gave; each item also shows FDA’s official class. Brand-new recalls appear in the daily digest first.
Source: RC-025‑2026-Retail-List.pdf (official USDA PDF)
WASHINGTON, Oct. 02, 2026, Inexport Logistics LLC, a Miami, Fla. firm, is recalling approximately 189 pounds of potato chip products containing chicharrón (pork cracklings) because they were produced in the Republic of Colombia, a country that is not eligible to export meat products to the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The following products are subject to recall, regardless of the product date [view labels]:
60-g. foil bags of “YUPI GOLPE CON TODO SABOR BBQ” mixed chips with “Clásicas,” “PLATANOS,” and “Chicharrón Fred.”
The products subject to the recall do not bear any import marks on the labels. These items were shipped to distributors and retail locations in Arizona, California, Colorado, Florida, Illinois, Kentucky, Minnesota, and Texas.
The problem was discovered during an FSIS recall effectiveness check where the ineligible product was observed in a retail location.
There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about illness or injury should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify theircustomers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Mauricio Caro, Sales Manager of Inexport Logistics LLC, at (786) 670‑4750 or sales@inexportlogistics.com.
Last updated by USDA: Oct 08, 2026
Source: RC-024‑2026-Retail-List.pdf (official USDA PDF)
WASHINGTON, Sept. 25, 2026 – Sempio Food Services Inc., located in Cerritos, Calif., is recalling approximately 4,596 pounds of ready-to-eat chicken stew products that were imported from the Republic of Korea without the benefit of import reinspection into the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The chicken stew products were produced on March 30, 2026, and have best-by date of September 29, 2027. The following products are subject to recall [view labels]:
Cardboard boxes containing pouches of 31.75-oz (900 g) “Sempio Korean Ginseng CHICKEN STEW CLASSIC”
Cardboard boxes containing pouches of 31.75-oz (900 g) “Sempio Korean Ginseng CHICKEN STEW RICH”
The products subject to the recall bear Korean establishment number “GIA15001” and shipping mark “MK-2026‑0422‑01”. The products were distributed to distributors and retailers in Florida, Georgia, Illinois, Maryland, New Jersey, New York, Pennsylvania and Virginia.
The problem was discovered during routine FSIS surveillance activities.
There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about an illness or injury should contact a healthcare provider.
FSIS is concerned that some product may be in in consumers’ pantries. Consumers who have purchased these products are urged not to consume them. Retailers are urged not to sell these products. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Media and consumers with questions regarding the recall can contact Daniel Park, President, Sempio Food Services, USA, at 562‑207‑9540, Ext. 101 or dypark3438@sempiofs.net.
Last updated by USDA: Oct 08, 2026
Source: RC-023‑2026-Retail-List.pdf (official USDA PDF)
WASHINGTON, Sept. 25, 2026 – Fontanini Foods LLC, a McCook, Ill., establishment, is recalling approximately 2,320 pounds of raw, frozen pork breakfast sausage products that may be contaminated with foreign material, specifically clear, hard plastic, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The raw, frozen pork breakfast sausage items were produced on June 23, 2026. The following products are subject to recall [view labels]:
10-lb. cardboard box cases containing “Fontanini PORK SAUSAGE LINKS” with “ITEM 393” printed on the box and “PACKED ON 06/23/2026” printed on the shipping label.
The products subject to recall bear establishment number “EST. 6944” inside the USDA mark of inspection printed on the box. These items were shipped to distributors in California, Florida, Michigan, and Nevada to be served in food service establishments, including restaurants.
The problem was discovered after the firm received two customer complaints regarding clear, hard plastic found in the sausage product.
There have been no confirmed reports of injury or adverse reactions due to consumption of these products. Anyone concerned about an injury should contact a healthcare provider.
FSIS is concerned that some product may be in food service and restaurant freezers. Food service establishments and restaurants are urged not to serve this product. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify theircustomers of the recall and that steps are taken to make certain that the product is no longer available to consumers. If any specific retail locations are identified, a distribution list will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers, foodservice operators, and members of the media with questions about the recall can contact Fontanini Foods at media@hormel.com.
Last updated by USDA: Oct 08, 2026
Source: RC-022‑2026-Retail-List.pdf (official USDA PDF)
WASHINGTON, Sept. 22, 2026 – Star Meat Delivery Inc., located in Lucama, N.C., is recalling approximately 167,639 pounds of raw pork, beef, and goat products that were produced without the benefit of federal inspection, bearing labels with a false USDA mark of inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. As more information becomes available, FSIS may update the product list and labels with additional items.
Any product bearing the false establishment number “EST. 1363” should be considered misbranded and unsafe to eat.
The raw pork, beef, and goat items were produced on various dates prior to September 22, 2026. The products were vacuum-sealed and packed into cardboard boxes for shipment; individual consumer packages may not bear this labeling, as retail stores may have applied their own stickers with pricing and safe handling instructions. The following products, distributed in bulk under the A&D Foods label, are subject to recall [view currently available labels]:
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “GOAT CUT 1‑1/2" 10.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “GOAT BURN SKIN ON CUT 1‑1/2" 10.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “SLICE RIBEYE 4oz 10.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “BEEF CHUCK THIN SLICED KBQ 4 MM 20.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “BEEF OXTAIL CUT 10.00LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “BEEF SHORT RIBS SLD 3/8" REGULAR 10.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “SHANKS BONE IN CUT 1.5 10.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “PORK GROUND 10.00LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “PORK CHORIZO 10.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “PORK CHOP B/I 10.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “PORK FEET CUT 8 PCS 10.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “PORK FEET CUT 6 PCS 10.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “PORK RIB PIECES PREM 1" 10.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “PORK BOSTON DICED 10.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “PORK BOSTON SLICE 1 INCH 20.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “Menudo Mix 30.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “PORK BOSTON THIN SLICED 3.5MM 20.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods “PORK HOCK SLICED 10.00 LBS”
Various weight cardboard boxes containing individually vacuum-packed A&D Foods Beef Ribs 4Bone 2" C. Cut P/Caldo
Various weight cardboard boxes containing individually vacuum-packed A&D Foods Beef Short Rib Thin Sliced
Various weight cardboard boxes containing individually vacuum-packed A&D Foods Pork Boston Butt Sliced 4MM
Various weight cardboard boxes containing individually vacuum-packed A&D Foods Beef Short Ribs SLD 3/8" Premium C. Cut
Various weight cardboard boxes containing individually vacuum-packed A&D Foods Beef Feet Cut
The products subject to recall bear false marks of inspection with establishment number “EST. 1363,” which does not have a federal grant of inspection. These items were shipped to A&D Foods, a distributor in Georgia, for further distribution to retail and restaurant locations nationwide.
The problem was discovered during FSIS surveillance activities.
There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about an illness or injury should contact a healthcare provider.
Food produced without inspection may contain undeclared allergens, harmful bacteria, or other contaminants that put consumer health and safety at risk. FSIS is concerned that some product may be in the refrigerators or freezers of consumers, restaurants, or retailers. Consumers who have purchased these products are urged not to consume them. Retailers and restaurants are urged not to sell or serve these products. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Jennifer Joyner, Media Office Manager, Star Meat Delivery Inc. at 252‑239‑0610 or starmeatdelivery@gmail.com.
Last updated by USDA: Sep 28, 2026
Source: RC-021‑2026-Retail-List.pdf (official USDA PDF)
Editor's Note: This release was updated on September 17, 2026, to add additional states, including Massachusetts, New York, Connecticut, and Illinois, and to remove the specific July 28 import date to more accurately characterize the product as ineligible for import.WASHINGTON, Sept. 09, 2026, El Eden Import Distributor Corp., a Long Island City, N.Y. firm, is recalling approximately 264 pounds of potato chip products containing chicharrón (pork cracklings) because they were produced in the Republic of Colombia, a country that is not eligible to export meat products to the United States, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today.The following products are subject to recall [view labels]:45-g. foil bags of “De Todito NATURAL” mixed chips with “CHICHARRÓN AMERICANO JACKS,” “Margarita,” and “NATU CHIPS.”45-g. foil bags of “De Todito BBQ” mixed chips with “CHICHARRÓN AMERICANO JACKS,” “Margarita,” and “NatuChips.”The products subject to the recall do not bear any import marks on the labels. These items were shipped to a distributor in New Jersey and retail locations in New Jersey, Utah, Massachusetts, New York, Connecticut, and Illinois. Please note, it may be possible as FSIS continues their investigation consignees in additional states may be identified.The problem was discovered when FSIS received a consumer complaint regarding “De Todito” snack products containing dried plantains, potato chips, and chicharrónes, pork cracklings, imported from Colombia, which is ineligible to import any meat or poultry product into the U.S.There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about illness or injury should contact a healthcare provider.FSIS is concerned that some product may be in consumers' pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.Consumers and members of the media with questions about the recall can contact Humberto Gallego, Owner, El Eden Import Distributor Corp. at Hhgl1968@gmail.com.
Last updated by USDA: Sep 17, 2026
Source: RC-019‑2026-Retail-List.pdf (official USDA PDF)
Source: RC-020‑2026-Retail-List.pdf (official USDA PDF)
WASHINGTON, Sept. 06, 2026 – Prime Line Distributors, Inc., a Fort Lauderdale, Fla., firm, and Ferrarini USA, Inc., a Hoboken, N.J., firm, are recalling approximately 1,513 pounds of imported ready-to-eat (RTE) pork products that may be adulterated with Listeria monocytogenes (Lm), the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The imported RTE dry-cured pork jowl (“guanciale”) products were produced at Est. 1937L Bome SRL in Italy on May 21, 2026, and imported into the U.S. on various dates within July 2026. The following products are subject to recall [view labels]:
Prime Line Distributors, Inc.:
Various weight cardboard cases containing two pieces of individually vacuumed packed “PRIME LINE DISTRIBUTORS, INC. GUANCIALE PORK JOWL PRODUCT OF ITALY” with “LOT: 263311US” and “BEST IF USE BY DATE: 05.16.27” printed on the label.
Various weight individually vacuumed packaged “GUANCIALE PORK JOWL PRODUCT OF ITALY” with “LOT: 263311US” and “BEST IF USE BY: 05.16.27” printed on the label. The product has an additional label with “DOK GUANCIALE” on the packaging.
Ferrarini USA, Inc.:
Various weight cardboard cases containing two pieces of individually vacuumed packed “GUANCIALE PORK JOWL PRODUCT OF ITALY” with “LOT: 263311US” and “BEST IF USE BY DATE: 05.16.27” printed on the label.
Various weight individually vacuumed packaged “FERRARINI GUANCIALE DRY-CURED PORK JOWL” with “LOT: 263311US” and “BEST IF USE BY DATE: 05.16.27” printed on the label.
The products subject to recall bear establishment number “IT 1937 L CE” inside the Italian mark of inspection or printed on the case label. The Prime Line Distributors, Inc., items were shipped to food service and retail locations in Florida. The Ferrarini USA, Inc. items were shipped to distributors and food service locations in California, Florida, Idaho, Illinois, Michigan, New Jersey, New York and Texas.
The problem was discovered during routine import reinspection testing when a product sample confirmed positive for Listeria monocytogenes (Lm).
There have been no confirmed reports of illness due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
Consumption of food contaminated with Lm can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS is concerned that some products may be in food service and retail refrigerators and freezers. Food service and retail locations are urged not to serve or sell these products. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify theircustomers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Media and consumers with questions about the affected Prime Line Distributors, Inc., products can contact Liliana Rojas, QA/QC Manager, at 954‑925‑4500 or Liliana.rojas@primelinedist.com.
Media and consumers with questions about the affected Ferrarini USA, Inc., products can contact Luca Infantino, Chief Financial Officer, at 818‑256‑1622 or Luca@ferrariniusa.com.
Last updated by USDA: Sep 29, 2026
Source: RC-017‑2026-Retail-List.pdf (official USDA PDF)
WASHINGTON, Aug. 17, 2026 – Indus Foods, LLC, doing business as Gangothri Foods, an Austin, Tex. firm, is recalling approximately 1,626 pounds of ready-to-eat (RTE) pickled goat and chicken products that were produced without the benefit of inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The RTE pickled goat and chicken products were produced between January 28, 2025, and May 6, 2026, and have a two-year shelf life. The following products are subject to recall [view labels]:
8-oz. glass jars containing “Gangothri Goat Pickle”
8-oz. glass jars containing “Gangothri Gongura Goat Pickle”
8-oz. glass jars containing “Gangothri Chicken Pickle”
8-oz. glass jars containing “Gangothri Gongura Chicken Pickle”
The products subject to recall do not bear a USDA mark of inspection. The affected products were sold to restaurants, retail locations, and distributors nationwide and direct to consumers online.
The problem was discovered during FSIS surveillance activities There have been no confirmed reports of illness due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ pantries or on restaurant and distributor shelves. Consumers who have purchased these products are urged not to consume them, and restaurants and distributors are urged not to serve or sell them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify theircustomers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Media and consumers with questions regarding the recall can contact Jyothi Yerramreddy at 512‑284‑7790 or Gangothripickles@gmail.com.
Last updated by USDA: Aug 17, 2026
Source: RC-014‑2026-Retail-List.pdf (official USDA PDF)
WASHINGTON, Aug. 7, 2026 – Shan Distribution Network, Inc., located in Carol Stream, Ill., is recalling approximately 5,084 pounds of frozen Siluriformes breaded Swai fish fillet and stick products because they were produced in the United Arab Emirates, a country that is not eligible to export Siluriformes fish to the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The frozen Siluriformes breaded Swai fish fillet and stick products were produced in December 2025, and have use before dates in June 2027. The following products are subject to recall [view labels]:
13.75-oz. boxes containing Al Kabeer spicy “Zing Fish Fillets Breaded Partially Cooked Swai Fish Fillets”
10.58-oz. boxes containing Al Kabeer “Fish Sticks Breaded Swai Fish”
330-g boxes containing Al Kabeer “Breaded Fish Fillets”
The products do not bear an establishment number nor a USDA mark of inspection. These items were shipped to retail locations in Illinois, Indiana, Iowa, Michigan, Minnesota, Missouri, Ohio, and Wisconsin.
The problem was discovered during routine FSIS inspection activities.
There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about an illness or injury should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators and freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Shaheen James, Office Manager, Shan Distribution Network, Inc., at 630‑480‑0616 or shaheen.sdn@gmail.com.
Last updated by USDA: Aug 07, 2026
Source: RC-013‑2026-Retail-List.pdf (official USDA PDF)
WASHINGTON, Aug. 7, 2026 – Corte Argentino USA LLC, located in Aventura, Fla., is recalling approximately 29,628 pounds of raw beef products that were imported from Argentina without the benefit of import reinspection into the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The raw beef products were produced between May 15, 2026, and May 20, 2026, and have use or freeze-by dates between September 15, 2026, and September 20, 2026. The following products are subject to recall [view labels]:
Various weight cardboard boxes containing “FrigorIfico Gorina SAIC” boneless beef “Top Sirloin Butt” (“Cuadril Sin Tapa”)
Various weight cardboard boxes containing “FrigorIfico Gorina SAIC” boneless beef “Eye Round” (“Peceto”)
Various weight cardboard boxes containing “FrigorIfico Gorina SAIC” boneless beef “Topside Cap Off” (“Nalga AD S/Tapa”)
Various weight cardboard boxes containing “FrigorIfico Gorina SAIC” boneless beef “Flat” (“Carnaza Cuadrada”)
Various weight cardboard boxes containing “FrigorIfico Gorina SAIC” boneless beef “Knuckle” (“Bola de Lomo”)
The products subject to the recall bear Argentinian establishment number “EST. N° OF. 2025” and shipping mark “26644-AA” The products were distributed to distributors and retailers in Florida and Texas.
The problem was discovered during routine FSIS inspection activities.
There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about an illness or injury should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators and freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify theircustomers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Eial Kaplun, General Manager, Corte Argentino USA LLC, at 786‑350‑5805 or info@corteargentinoinc.com.
Last updated by USDA: Aug 24, 2026
Source: RC-011‑2026-Retail-List.pdf (official USDA PDF)
WASHINGTON, JULY 24, 2026 - Maple Leaf Foods, Inc., located in Lisle, Illinois, is recalling approximately 12,036 pounds of not ready-to-eat (NRTE) smoked bacon product that was imported from Canada without the benefit of import reinspection into the United States, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today.The NRTE refrigerated smoked bacon product was produced June 9, 2026, June 10, 2026, June 12, 2026, June 13, 2026, and June 15, 2026. The following products are subject to recall [view labels]:12-oz vacuum package of "Royale Natural Applewood Smoked ALL NATURAL Uncured Bacon Product of Canada" with sell by dates of "SEP 01 2026" and "SEP 07 2026" printed on the side of the package12-oz vacuum package of "TOP VALU Uncured Hardwood Smoked Bacon PRODUCT OF CANADA" with various sell by dates of "SEP 01 2026", "SEP 02 2026", "SEP 04 2026", "SEP 05 2026", and "SEP 07 2026" printed on the side of the packageThe product subject to recall bears Canadian establishment number "EST. 1" printed on the side the package, and health certificate "2026-S732971612" on master case boxes. This item was further distributed to Grocery Outlet distributors and retailers in Idaho, Oregon, and Washington.The problem was discovered during routine FSIS inspection activities.There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about an illness or injury should contact a healthcare provider.FSIS is concerned that some product may be in consumers' refrigerators and freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.Media and consumers with questions regarding the public health alert can contact Adam Emery, Vice President, Communications, Maple Leaf Foods, Inc., at 416‑518‑5131 or adam.emery@mapleleaf.com.
Last updated by USDA: Jul 24, 2026
Source: RC-010‑2026-Retail-List.pdf (official USDA PDF)
WASHINGTON, JULY 23, 2026 - BCI Foods, Inc., the importer of record located in Saint-Hyacinthe, Quebec, Canada, is recalling approximately 4,300 pounds of a chicken noodle soup product that was imported from Canada without the benefit of import reinspection into the United States, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today.The canned condensed chicken noodle soup product was produced on February 4, 2026. The following product is subject to recall [view labels]:10.5-oz can of "tasty KITCHEN Chicken Noodle Condensed Soup PRODUCT OF CANADA" with best by date of "2028 FE 04" and lot code "5 9 2 26 035"The product subject to recall bears Canadian establishment number "EST. 142" printed on the can. This item was further distributed to food banks and food pantry locations in Oklahoma.The problem was discovered when the firm notified FSIS that the canned chicken soup product imported from Canada was not presented for FSIS import reinspection.There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about an illness or injury should contact a healthcare provider.FSIS is concerned that some product may be in consumers' pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.Media and consumers with questions regarding the public health alert can contact Marie-Lou Corbin, Vice President, Sales, BCI Foods, Inc., at 514‑218‑7143 or marie-lou.corbin@bcifoods.com.
Last updated by USDA: Jul 23, 2026
Store list: not posted by USDA
WASHINGTON, June 18, 2026 - Power Plate Meals, LLC, a West Fargo, N.D. Cooperative Interstate Shipping establishment, is recalling approximately 5,795 pounds of frozen meatloaf with garlic mashed potatoes products due to misbranding and an undeclared allergen, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today. The product contains soy, a known allergen, which is not declared on the product label.
The frozen meatloaf with garlic mashed potatoes items were produced June 25, 2025, to June 10, 2026. The following products are subject to recall [view labels]:
13.3-oz. vacuum sealed plastic tray packages containing "POWER PLATE MEALS MEATLOAF WITH GARLIC MASHED POTATOES" and "USE BY" dates between 6/25/26 and 6/10/27.
The products subject to recall bear establishment number "217SEND" inside the USDA mark of inspection. These items were shipped to distributors in Minnesota, North Dakota and South Dakota.
The problem was discovered when a state inspector notified FSIS that the final label did not contain soy in the ingredients list.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers' freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
Consumers and members of the media with questions about the recall can contact Power Plate Meals, LLC, customer service hungry2help@powerplatemeals.com.
Last updated by USDA: Jun 18, 2026
Reason (FDA): Salmonella
Where it went (FDA): Distributed in WA
Recalling firm: Evergreen Fresh Sprouts LLC, Moyie Springs, ID
FDA recall event 99842 · status Ongoing
FDA Enforcement Report → search event 99842
Reason (FDA): Contamination with Listeria monocytogenes
Where it went (FDA): Walmart DCs and retail locations nationwide.
Recalling firm: GIAS FOOD INC., New York, NY
FDA recall event 99853 · status Ongoing
FDA Enforcement Report → search event 99853
Reason (FDA): Potential E. coli O145:H28 Contamination
Where it went (FDA): AR
Recalling firm: Frutas y Hortalizas del Sur S.A., San Carlos, N/A
FDA recall event 99831 · status Ongoing
FDA Enforcement Report → search event 99831
Reason (FDA): Potential Salmonella contamination
Where it went (FDA): Nationwide US and UAE. The recalled organic moringa leaf powder was distributed nationwide in retail stores and through online sellers including but not limited to www.foodsalive.com.
Recalling firm: FOODS ALIVE INC., Angola, IN
FDA recall event 99830 · status Ongoing
FDA Enforcement Report → search event 99830
Reason (FDA): The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes.
Where it went (FDA): Florida
Recalling firm: Optimus Inc. d/b/a/ Markys Caviar, Miami Gardens, FL
FDA recall event 99841 · status Ongoing
FDA Enforcement Report → search event 99841
Reason (FDA): Potential E. coli and Salmonella contamination
Where it went (FDA): Wholesale consignees in 16 states: CA, FL, HI, IL, MA, MN, MO, MT, NY, OH, OR, PA, TN, SC, TX, UT; Puerto Rico; Canada, Mexico, Tahiti, and Venezuela
Recalling firm: International Sprout Holdings, Inc, Cookeville, TN
FDA recall event 99822 · status Ongoing
FDA Enforcement Report → search event 99822
Reason (FDA): Sprouts may be contaminated with STEC E. coli and/or Salmonella.
Where it went (FDA): MN, WI
Recalling firm: Everything Sprouts, LLC, Minneapolis, MN
FDA recall event 99737 · status Ongoing
FDA Enforcement Report → search event 99737
Reason (FDA): Product may be contaminated with Salmonella
Where it went (FDA): CT, NY, NJ, and PA
Recalling firm: Panorama Produce Sales Inc., Mamaroneck, NY
FDA recall event 99780 · status Ongoing
FDA Enforcement Report → search event 99780
Reason (FDA): Product may be contaminated with Salmonella.
Where it went (FDA): Nationwide
Recalling firm: THE HAMPTON GROCER, Montauk, NY
FDA recall event 99656 · status Ongoing
FDA Enforcement Report → search event 99656
Reason (FDA): Product had a presumptive positive test result for Listeria monocytogenes
Where it went (FDA): The recalled product was distributed to the following States: IL, NV, NM, CA, OK, TX, PA, OH, NC, NY, GA, and AR.
Recalling firm: CUISINE, KETTLE, Savage, MD
FDA recall event 99690 · status Ongoing
FDA Enforcement Report → search event 99690
Reason (FDA): Salmonella. The firm received a positive test result of Salmonella in the product.
Where it went (FDA): Washington DC, DE, GA, MD, NC, NJ, NY, PA, SC, VA.
Recalling firm: Lidl US TRADING, Arlington, VA
FDA recall event 99618 · status Ongoing
FDA Enforcement Report → search event 99618
Reason (FDA): Potential contamination with Salmonella.
Where it went (FDA): Domestic: AL, AR, FL, GA, IL, IN, KS, KY, LA, MA, ME, MI, MN, MO, MS, NC, NE, NH, NY, OH, OK, SC, TN, TX, VT, WI, WV. Foreign: Not applicable.
Recalling firm: Taylor Fresh Foods Inc, Salinas, CA
FDA recall event 99611 · status Ongoing
FDA Enforcement Report → search event 99611
Reason (FDA): Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Where it went (FDA): AR, IA, IL, IN, KY, LA, MI, MN, MO, OH, OK, TX, WI
Recalling firm: WFM Purchasing, LP, Austin, TX
FDA recall event 99640 · status Ongoing
FDA Enforcement Report → search event 99640
Reason (FDA): Jalapenos have the potential to be contaminated with Salmonella
Where it went (FDA): Texas and Louisiana
Recalling firm: NatureBest Pre-Cut & Produce LLc, Missouri City, TX
FDA recall event 99594 · status Ongoing
FDA Enforcement Report → search event 99594
Reason (FDA): Jalapenos may be contaminated with Salmonella.
Where it went (FDA): LA, TX
Recalling firm: Dairyland Produce, LLC, Dallas, TX
FDA recall event 99635 · status Ongoing
FDA Enforcement Report → search event 99635
Reason (FDA): Potential Salmonella contamination
Where it went (FDA): IL, IN, MI, WI
Recalling firm: GET FRESH PRODUCE, Bartlett, IL
FDA recall event 99650 · status Ongoing
FDA Enforcement Report → search event 99650
Reason (FDA): Potential Salmonella Javiana contamination
Where it went (FDA): OH, PA (for food service use only)
Recalling firm: Sirna and Sons Produce, Inc, Ravenna, OH
FDA recall event 99695 · status Ongoing
FDA Enforcement Report → search event 99695
Reason (FDA): Potential Listeria contamination from dripping condensation in cooler.
Where it went (FDA): WI
Recalling firm: Elegant Foods, LLC, Madison, WI
FDA recall event 99702 · status Ongoing
FDA Enforcement Report → search event 99702
Reason (FDA): The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Where it went (FDA): The recall product was distributed to the following States: PA, MD, NY, CT, NJ
Recalling firm: Buckhead Meat Company D.B.A. Trinity Seafood, Lakewood, NJ
FDA recall event 99744 · status Ongoing
FDA Enforcement Report → search event 99744
Reason (FDA): Potential Salmonella Javiana contamination
Where it went (FDA): Products were distributed primarily to wholesale distributors in the central and east coast states. Product has been further distributed nationwide and is packaged in bulk containers intended for further processing. No retail distribution has been identified as of 08/10/2026.
Recalling firm: Coast Citrus Distributors, San Diego, CA
FDA recall event 99569 · status Ongoing
FDA Enforcement Report → search event 99569
Reason (FDA): Possible Salmonella in Moringa Leaf Powder product.
Where it went (FDA): Distributed to Nevada for further distribution.
Recalling firm: FACTORY6, INC., Lindon, UT
FDA recall event 99425 · status Ongoing
FDA Enforcement Report → search event 99425
Reason (FDA): Potential Cyclospora contamination.
Where it went (FDA): Domestic: AL, AR, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NH, NJ, OH, OK, PA, SC, TN, TX, VA, and WI. (Subway distribution limited to: AR, LA, and TX) Foreign: Mexico.
Recalling firm: Taylor Farms de Mexico S. de R.L. de C.V., Doctor Mora
FDA recall event 99453 · status Ongoing
FDA Enforcement Report → search event 99453
Reason (FDA): Product may be contaminated with Salmonella.
Where it went (FDA): Alabama, Alaska, Arizona, Colorado, Florida, Georgia, Idaho, Kansas, Mississippi, Missouri, Montana, Nebraska, Nevada, New Mexico, Oregon, South Dakota, Tennessee, Washington, and Wyoming
Recalling firm: Botticelli Foods, LLC, Hauppauge, NY
FDA recall event 99538 · status Ongoing
FDA Enforcement Report → search event 99538
Reason (FDA): Moringa Powder ingredient positive for salmonella
Where it went (FDA): Product was distributed to 4 different consignees who have used the ingredient for further processing and distribution.
Recalling firm: Green Jeeva LLC, Cerritos, CA
FDA recall event 99387 · status Ongoing
FDA Enforcement Report → search event 99387
Reason (FDA): Potential E. coli O145:H28 Contamination
Where it went (FDA): FL
Recalling firm: Frutas y Hortalizas del Sur S.A., San Carlos
FDA recall event 99373 · status Ongoing
FDA Enforcement Report → search event 99373
Reason (FDA): Contaminated with Salmonella
Where it went (FDA): nationwide
Recalling firm: Total Nutrition Inc, Deer Park, NY
FDA recall event 99317 · status Ongoing
FDA Enforcement Report → search event 99317
Reason (FDA): Potential contamination with Salmonella
Where it went (FDA): NY
Recalling firm: Trafa Pharmaceutical Inc., Chicopee, MA
FDA recall event 99314 · status Ongoing
FDA Enforcement Report → search event 99314
Reason (FDA): Product may be contaminated with Clostridium botulinum.
Where it went (FDA): nationwide
Recalling firm: NARA ORGANICS INC, New York, NY
FDA recall event 99242 · status Ongoing
FDA Enforcement Report → search event 99242
Reason (FDA): Products may be contaminated with Listeria monocytogenes.
Where it went (FDA): Only in NY.
Recalling firm: Nelson & Isa Lacteos LLC, Bay Shore, NY
FDA recall event 99142 · status Ongoing
FDA Enforcement Report → search event 99142
Reason (FDA): Products may be contaminated with Listeria monocytogenes.
Where it went (FDA): The recalled product was distributed to the following states: MD, VA
Recalling firm: La Colonia Foods Llc, Rockville, MD
FDA recall event 99325 · status Ongoing
FDA Enforcement Report → search event 99325
Reason (FDA): Improperly eviscerated which may result in Clostridium botulinum contamination
Where it went (FDA): AZ, CA, FL, HI, IL, KS, LA, MD, MO, NC, NH, NV, NY, OK, OR, PA, TX, UT, WA
Recalling firm: Prime Food Processing LLC., Brooklyn, NY
FDA recall event 99147 · status Ongoing
FDA Enforcement Report → search event 99147
Reason (FDA): Product contaminated with Listeria monocytogenes.
Where it went (FDA): MD, VA, NY
Recalling firm: Clover Hill Dairy, LLC, Mechanicsville, MD
FDA recall event 99211 · status Ongoing
FDA Enforcement Report → search event 99211
Reason (FDA): Product may be contaminated with Salmonella Typhimurium
Where it went (FDA): Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)
Recalling firm: MOGO Moringa LLC, Saint Louis, MO
FDA recall event 99071 · status Ongoing
FDA Enforcement Report → search event 99071
Reason (FDA): Product may be contaminated with Salmonella.
Where it went (FDA): Nationwide
Recalling firm: Total Nutrition Inc, Deer Park, NY
FDA recall event 99072 · status Ongoing
FDA Enforcement Report → search event 99072
Reason (FDA): Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.
Where it went (FDA): Product was distributed to 3 California customers.
Recalling firm: IQ PRODUCE, LLC, Vernon, CA
FDA recall event 99001 · status Ongoing
FDA Enforcement Report → search event 99001
Reason (FDA): Un-eviscerated fish may be contaminated with clostridium botulinum
Where it went (FDA): MA, NJ, IL, and NY
Recalling firm: Terra Medi LLC, Long Island City, NY
FDA recall event 98989 · status Ongoing
FDA Enforcement Report → search event 98989
Reason (FDA): Imported Enoki Mushrooms tested positive for Listeria Monocytogenes.
Where it went (FDA): Product was distributed to a single customer located in Texas. Product was further distributed as samples were collected in Florida.
Recalling firm: HH FRESH TRADING CORP, Los Angeles, CA
FDA recall event 98993 · status Ongoing
FDA Enforcement Report → search event 98993
Reason (FDA): potential presence of Salmonella
Where it went (FDA): Nationwide
Recalling firm: JOHN B SANFILIPPO & SONS INC, Elgin, IL
FDA recall event 98919 · status Ongoing
FDA Enforcement Report → search event 98919
Reason (FDA): Products were made with recalled California Dairies milk powder due to Salmonella.
Where it went (FDA): PA, WI
Recalling firm: Legacy Bakehouse LLC, Waukesha, WI
FDA recall event 98928 · status Ongoing
FDA Enforcement Report → search event 98928
Reason (FDA): Product may be contaminated with Salmonella.
Where it went (FDA): NY, PA
Recalling firm: Stoltzfus Family Dairy LLC, Vernon Center, NY
FDA recall event 98934 · status Ongoing
FDA Enforcement Report → search event 98934
Reason (FDA): Potential contamination with Salmonella
Where it went (FDA): Domestic Distribution: OH. Foreign Distribution: N/A.
Recalling firm: Guittard Chocolate Company, Burlingame, CA
FDA recall event 98949 · status Ongoing
FDA Enforcement Report → search event 98949
Reason (FDA): Products may be potentially contaminated with Salmonella.
Where it went (FDA): KS, MN, NY, WI
Recalling firm: JCB Flavors, LLC, Watertown, WI
FDA recall event 98902 · status Ongoing
FDA Enforcement Report → search event 98902
Reason (FDA): Salmonella. The firm was notified by the North Carolina Department of Agriculture that the product test positive for Salmonella.
Where it went (FDA): Product was shipped to MI & NC.
Recalling firm: Nassar Investment Company LLC, Morrisville, NC
FDA recall event 98923 · status Ongoing
FDA Enforcement Report → search event 98923
Reason (FDA): Potential presence of Salmonella.
Where it went (FDA): The recalled product was distributed to the following states. AL,AR,AZ,CA,CO,CT,FL,GA,IA,IL,IN, KY, LA,MA,MD,ME,MI,MN,MO,MS,NC,NJ,NV,NY, OH,OK,OR,PA,SC,TN,TX,VA,VT,WI
Recalling firm: Utz Quality Foods, LLC, Hanover, PA
FDA recall event 98864 · status Ongoing
FDA Enforcement Report → search event 98864
Reason (FDA): Potential contamination with Salmonella.
Where it went (FDA): U.S. Distribution Pattern: AK, AZ, CA, FL, GA, ID, IL, IN, KY, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI. Foreign Distribution Pattern: Canada, Guatemala, Japan, Philippines, United Kingdom, South Korea.
Recalling firm: Ghirardelli Chocolate Company, San Leandro, CA
FDA recall event 98851 · status Ongoing
FDA Enforcement Report → search event 98851
Reason (FDA): potential to be contaminated with Salmonella
Where it went (FDA): MI WI PA IL GA CA KS
Recalling firm: Solina U.S. Holding, Eastvale, CA
FDA recall event 98844 · status Ongoing
FDA Enforcement Report → search event 98844
Reason (FDA): Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Where it went (FDA): Nationwide
Recalling firm: PS Seasoning & Spices, Inc., Iron Ridge, WI
FDA recall event 98822 · status Ongoing
FDA Enforcement Report → search event 98822
Reason (FDA): Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.
Where it went (FDA): Distribution is to California and Utah consignees.
Recalling firm: Honeyville, Inc, Ogden, UT
FDA recall event 98841 · status Ongoing
FDA Enforcement Report → search event 98841
Reason (FDA): Potential contamination with Salmonella.
Where it went (FDA): U.S. Distribution: Unknown and to be determined during RAC assignment. Domestic consignees pick-up product from CDI. Foreign Distribution: Mexico, Philippines, Dominican Republic.
Recalling firm: California Dairies Inc., Visalia, CA
FDA recall event 98796 · status Ongoing
FDA Enforcement Report → search event 98796
Reason (FDA): May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
Where it went (FDA): NY and online sales
Recalling firm: LIQUID BLENZ CORP, Rockville Centre, NY
FDA recall event 98765 · status Ongoing
FDA Enforcement Report → search event 98765
Reason (FDA): Multi-state outbreak of E. coli O157:H7.
Where it went (FDA): U.S. distribution: AZ, CA, CO, FL, GA, IL, IN, MD, NV, TX. Foreign distribution: None.
Recalling firm: Raw Farm LLC, Fresno, CA
FDA recall event 98703 · status Ongoing
FDA Enforcement Report → search event 98703
Reason (FDA): product tested positive for Listeria Monocytogenes.
Where it went (FDA): 5 direct account consignees located in CA, FL and MD.
Recalling firm: HEMU TRADING INC, Los Angeles, CA
FDA recall event 98725 · status Ongoing
FDA Enforcement Report → search event 98725
Reason (FDA): Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella.
Where it went (FDA): Product was shipped to the following states: AZ, CA, CO, FL, GA, IL, LA, MD, MI, NC, PA, SC, TN, TX & WA.
Recalling firm: Griffith Foods Inc., Alsip, IL
FDA recall event 98604 · status Ongoing
FDA Enforcement Report → search event 98604
Reason (FDA): Contaminated with Listeria monocytogenes
Where it went (FDA): MD
Recalling firm: SLADE GORTON & CO., INC., Waltham, MA
FDA recall event 98424 · status Ongoing
FDA Enforcement Report → search event 98424
Reason (FDA): Potential contamination with Salmonella.
Where it went (FDA): U.S. Distribution: CA, CO, CT, FL, GA, IA, IL, IN, KY, MA, MD, MS, NC, NH, NJ, NM, NV, NY, OH, OR, PA, TN, TX, VT, WA, WI. Foreign Distribution: None
Recalling firm: Navitas, LLC., San Rafael, CA
FDA recall event 98335 · status Ongoing
FDA Enforcement Report → search event 98335
Reason (FDA): Potential contamination with Salmonella.
Where it went (FDA): U.S. distribution: CA, CO, NY Foreign distribution: Canada
Recalling firm: Tradin Organics USA LLC, Aptos, CA
FDA recall event 98318 · status Ongoing
FDA Enforcement Report → search event 98318
Reason (FDA): Potential Salmonella contamination
Where it went (FDA): Nationwide
Recalling firm: Spring & Mulberry Inc., Raleigh, NC
FDA recall event 98281 · status Ongoing
FDA Enforcement Report → search event 98281
Reason (FDA): Mold contamination detected for raw material lots that were produced in July and used in finished goods.
Where it went (FDA): The product was distributed to the following states: TX, FL, CA, NC, MI, MN, VA, NJ, MA, OH, IL,AL, CT, TN, NY, MO, PA, RI, SC, OK, GA, MN, WI, NV, IN, IA, CO, LA, NC, OR, KY, DE,
Recalling firm: QUTEN RESEARCH INSTITIUTE LLC, Pine Brook, NJ
FDA recall event 98211 · status Ongoing
FDA Enforcement Report → search event 98211
Reason (FDA): Potential contamination with Salmonella.
Where it went (FDA): U.S. Distribution: None Foreign Distribution: Canada
Recalling firm: Sam Dry Fruits and Nuts Enterprises, Inc, Modesto, CA
FDA recall event 98120 · status Ongoing
FDA Enforcement Report → search event 98120
Reason (FDA): Products may be contaminated with Salmonella Richmond.
Where it went (FDA): MD, NC, WA, CT, PA
Recalling firm: Organic Living Superfoods Llc, Walpole, MA
FDA recall event 98089 · status Ongoing
FDA Enforcement Report → search event 98089
Reason (FDA): Potential contamination with Salmonella.
Where it went (FDA): U.S. Distribution: CA, NJ Foreign Distribution: Canada
Recalling firm: The Whole Herb Company, Inc., Sonoma, CA
FDA recall event 98043 · status Ongoing
FDA Enforcement Report → search event 98043
Reason (FDA): Contaminated with Clostridium botulinum
Where it went (FDA): nationwide
Recalling firm: ByHeart, INC., New York, NY
FDA recall event 97959 · status Ongoing
FDA Enforcement Report → search event 97959
Reason (FDA): Clostridium botulinum (uneviscerated fish)
Where it went (FDA): Distributed to walk-in customers of African Food on Wheels Inc. located at 1376 Randall Avenue, Bronx, NY 10474 only
Recalling firm: African Food on Wheels Inc., Bronx, NY
FDA recall event 97940 · status Ongoing
FDA Enforcement Report → search event 97940
Reason (FDA): May be contaminated with Clostridium botulinum
Where it went (FDA): CT, MA
Recalling firm: First & Last Tavern, Hartford, CT
FDA recall event 97906 · status Ongoing
FDA Enforcement Report → search event 97906
Reason (FDA): Product contains yellow oleander
Where it went (FDA): Product was distributed directly to consumers via internet sales in AZ, CA, NM, NY, TX, UT
Recalling firm: Siluetaya, LLC, Albuquerque, NM
FDA recall event 97947 · status Ongoing
FDA Enforcement Report → search event 97947
Reason (FDA): Un-eviscerated fish may be contaminated with Clostridia botulinum.
Where it went (FDA): NY, NJ
Recalling firm: New Hoque and Sons, Inc., Maspeth, NY
FDA recall event 97895 · status Ongoing
FDA Enforcement Report → search event 97895
Reason (FDA): Potential contamination of Salmonella Richmond
Where it went (FDA): Product was distributed to consignee locations across the country.
Recalling firm: MeriCal, LLC, Anaheim, CA
FDA recall event 97885 · status Ongoing
FDA Enforcement Report → search event 97885
Reason (FDA): Potential contamination with Listeria monocytogenes.
Where it went (FDA): U.S. Distribution: MN
Recalling firm: Del Mar Food Products Corp., Watsonville, CA
FDA recall event 97771 · status Ongoing
FDA Enforcement Report → search event 97771
Reason (FDA): Potential contamination with Listeria monocytogenes.
Where it went (FDA): TX, IN
Recalling firm: Nate's Fine Foods, LLC, Roseville, CA
FDA recall event 97791 · status Ongoing
FDA Enforcement Report → search event 97791
Reason (FDA): Fish is un-eviscerated (may be contaminated with Clostridia botulinum), is contaminated with mold, and contains filth (insect larvae)
Where it went (FDA): NY
Recalling firm: Vicky IT Inc., Brooklyn, NY
FDA recall event 97722 · status Ongoing
FDA Enforcement Report → search event 97722
Reason (FDA): pathogen Cyclospora cayetanensis
Where it went (FDA): Nationwide
Recalling firm: MAYEJ COMERCIALIZADORA S. de R.L. de C.V., Pueblo Acatzingo De Hidalgo
FDA recall event 97717 · status Ongoing
FDA Enforcement Report → search event 97717
Reason (FDA): Potential contamination with Listeria monocytogenes.
Where it went (FDA): CA, IN, PA, TX
Recalling firm: Nate's Fine Foods, LLC, Roseville, CA
FDA recall event 97697 · status Ongoing
FDA Enforcement Report → search event 97697
Reason (FDA): Potential yeast contamination.
Where it went (FDA): AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, NC, ND, NH, NJ, NY, OH, OR, PA, SC, TN, TX, UT, VA, WI
Recalling firm: M.O.M Enterprises, LLC., Richmond, CA
FDA recall event 97608 · status Ongoing
FDA Enforcement Report → search event 97608
Reason (FDA): The firm had a positive Listeria Monocytogenes on a sample from this batch of product made.
Where it went (FDA): The recalled product was distributed to the following states: CT, NJ, MT, VA
Recalling firm: GOOT ESSA, LLC, Howard, PA
FDA recall event 97642 · status Ongoing
FDA Enforcement Report → search event 97642
Reason (FDA): Mold. The firm noticed an increase in customer complaints. They conducted a root cause investigation and discovered that one of their coolers had malfunctioning.
Where it went (FDA): Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV & WY.
Recalling firm: The J.M. Smucker Company, Orrville, OH
FDA recall event 97478 · status Ongoing
FDA Enforcement Report → search event 97478
Reason (FDA): Potential for spoilage due to yeast contamination.
Where it went (FDA): AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OH, OR, PA, RI, SC, TN, TX, VA, WI
Recalling firm: M.O.M Enterprises, LLC., Richmond, CA
FDA recall event 97401 · status Ongoing
FDA Enforcement Report → search event 97401
Reason (FDA): Listeria monocytogenes. During routine testing the firm received positive test results for Listeria monocytogenes.
Where it went (FDA): Product was shipped to the following: Distribution Center Shipped to: AR, AZ, CO, KS, IL, IN, MN, TX Distribution Centers Provided to these states: AL, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, LA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, PA, PR, SC, SD, TN, TX, UT, VA, WI, WV, WY
Recalling firm: Doehler North America, Inc., Cartersville, GA
FDA recall event 97340 · status Ongoing
FDA Enforcement Report → search event 97340
Reason (FDA): Salmonella. The firm was notified by the FDA that the product may be contaminated with Salmonella.
Where it went (FDA): Product was shipped to the following states: AL, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NC, NE, NH, NJ, OH, OK, PA, SC, SD, TN, TX, VA, WA & WI.
Recalling firm: World Market Management Services, LLC, Alameda, CA
FDA recall event 97240 · status Ongoing
FDA Enforcement Report → search event 97240
Reason (FDA): contaminated with Bacillus cereus and may be spoiled
Where it went (FDA): Nationwide
Recalling firm: Prestige Brands Holdings, Tarrytown, NY
FDA recall event 97088 · status Ongoing
FDA Enforcement Report → search event 97088
Reason (FDA): Potential contamination with Salmonella.
Where it went (FDA): AZ, CA, IL, IN, NE, NM, NV, WA, WY
Recalling firm: August Egg Company, Hilmar, CA
FDA recall event 97040 · status Ongoing
FDA Enforcement Report → search event 97040
Reason (FDA): The recall was the result of the firm's routine sampling program and Listeria monocytogenes was detected in an in-process shrimp sample in a food production environment.
Where it went (FDA): Distributed nationwide and in Canada.
Recalling firm: Bornstein Seafoods Inc, Astoria, OR
FDA recall event 97038 · status Ongoing
FDA Enforcement Report → search event 97038
Reason (FDA): Salmonella. The firm received cucumbers produced by Bedner Farms.
Where it went (FDA): Product was shipped to the following states: KY, NC, OH, VA & WV.
Recalling firm: Ukrop's Homestyle Foods LLC, North Chesterfield, VA
FDA recall event 96931 · status Ongoing
FDA Enforcement Report → search event 96931
Reason (FDA): Cucumbers have the potential to be contaminated with Salmonella.
Where it went (FDA): AL, IL, IN, KY, MI, TN, WI
Recalling firm: JFE FRANCHISING INC, Houston, TX
FDA recall event 96933 · status Ongoing
FDA Enforcement Report → search event 96933
Reason (FDA): Product may contain Salmonella.
Where it went (FDA): Product was shipped to the following states: GA, NC & SC.
Recalling firm: Williams Farms Produce Sales Co., Inc., Lodge, SC
FDA recall event 96800 · status Ongoing
FDA Enforcement Report → search event 96800
Reason (FDA): Potential contamination with Listeria monocytogenes.
Where it went (FDA): Distribution centers located throughout the U.S. and further distributed to sensitive populations located in long term care facilities, skilled nursing homes, hospitals, etc.
Recalling firm: Lyons Magnus LLC, Fresno, CA
FDA recall event 96376 · status Ongoing
FDA Enforcement Report → search event 96376
Reason (FDA): The firm received complaints of spoilage and illness with the use of the products.
Where it went (FDA): The product was shipped to the following states: AL, AR, CO, CT, FL, GA, IL, IN, KY, LA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NY, OH, OK, PA, SC, TN, TX, VA, WI & WY.
Recalling firm: DANONE WAVE, Louisville, CO
FDA recall event 96378 · status Ongoing
FDA Enforcement Report → search event 96378
Reason (FDA): Sprouts have the potential to be contaminated with Listeria monocytogenes
Where it went (FDA): IA, MN, WI
Recalling firm: Jack & The Green Sprouts, Inc., River Falls, WI
FDA recall event 96257 · status Ongoing
FDA Enforcement Report → search event 96257
Reason (FDA): Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Where it went (FDA): Product was distributed nationwide.
Recalling firm: Chicken of the Sea; Thai Union, El Segundo, CA
FDA recall event 96258 · status Ongoing
FDA Enforcement Report → search event 96258
Reason (FDA): Potential contamination with Listeria monocytogenes.
Where it went (FDA): Walmart retail stores: AK, AR, AZ, CA, CO, ID, IL, IN, KY, LA, MI, MT, NV, OH, OK, OR, TX, UT, WA, WY
Recalling firm: Braga Fresh Foods LLC, Salinas, CA
FDA recall event 96081 · status Ongoing
FDA Enforcement Report → search event 96081
Reason (FDA): Potential contamination with Listeria monocytogenes.
Where it went (FDA): Product distributed to two (2) distribution centers in Texas (Dallas, Houston).
Recalling firm: Braga Fresh Foods LLC, Salinas, CA
FDA recall event 95989 · status Ongoing
FDA Enforcement Report → search event 95989
Reason (FDA): Possible contamination with Salmonella spp.
Where it went (FDA): Statewide distribution to MI, MO, OH, TX, VA, 4 locations received product via 3rd party truck. No foreign distribution and none to government agencies.
Recalling firm: Eagle Produce LLC, dba Martori Farms, Scottsdale, AZ
FDA recall event 95309 · status Ongoing
FDA Enforcement Report → search event 95309
Reason (FDA): Listeria monocytogenes
Where it went (FDA): KY MI OH WV
Recalling firm: JFE FRANCHISING INC, Houston, TX
FDA recall event 95034 · status Ongoing
FDA Enforcement Report → search event 95034
Reason (FDA): Potential E. coli O157:H7 contamination.
Where it went (FDA): U.S. distribution to the following: CA and WA No foreign distribution
Recalling firm: Gibson Farms Inc, Hollister, CA
FDA recall event 94521 · status Ongoing
FDA Enforcement Report → search event 94521
Reason (FDA): Possible contamination with Listeria monocytogenes
Where it went (FDA): Distributed to consumers nationwide
Recalling firm: Nutrition Corp, Moosic, PA
FDA recall event 94601 · status Ongoing
FDA Enforcement Report → search event 94601
Reason (FDA): FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans.
Where it went (FDA): Product is sold through authorized dealers and E-commerce throughout the USA and Mexico, While the products, Elv Control Herbal Supplement and Mexican Tejocote Root Supplement Pieces (Raiz de Tejocote Mexicano Suplemento en Trozos), were intended to be distributed only through authorized distributors, it is possible that these products were purchased and further distributed via e-commerce platforms and/ or physical stores.
Recalling firm: World Green Nutrition Inc., San Antonio, TX
FDA recall event 94346 · status Ongoing
FDA Enforcement Report → search event 94346
Reason (FDA): Product is being recalled due to the presence of yellow oleander and its components in the product.
Where it went (FDA): Firm is 100% internet sales. Distribution is unknown at this time.
Recalling firm: HandNatural, San Luis, AZ
FDA recall event 93920 · status Ongoing
FDA Enforcement Report → search event 93920
Reason (FDA): Listeria monocytogenes contamination.
Where it went (FDA): U.S. distribution to the following: AR, AZ, BC, CA, CO, FL, GA, IA, IL, KS, MD, NC,NJ, NV, NY, OR, RI, TX, UT, VA, WA, W No foreign distribution.
Recalling firm: Rizo Lopez Foods, Inc. dba Don Francisco Cheese, Modesto, CA
FDA recall event 93814 · status Ongoing
FDA Enforcement Report → search event 93814
Reason (FDA): Listeria monocytogenes
Where it went (FDA): distributed nationwide in the US and in Costa Rica, China, and Japan.
Recalling firm: Twin City Foods, Inc., Stanwood, WA
FDA recall event 92907 · status Ongoing
FDA Enforcement Report → search event 92907
Reason (FDA): potential contamination with E coli
Where it went (FDA): Distributed to single consignee in California
Recalling firm: Global Vitality Inc., Chandler, AZ
FDA recall event 92751 · status Ongoing
FDA Enforcement Report → search event 92751
Reason (FDA): The firm was notified by their Brie Cheese supplier that the product may be contaminated with Listeria monocytogenes.
Where it went (FDA): Product was shipped to one distributor in Georgia
Recalling firm: Kabobs Acquisition Inc., Lake City, GA
FDA recall event 90951 · status Ongoing
FDA Enforcement Report → search event 90951
Reason (FDA): Cans of soda may contain yeast.
Where it went (FDA): IL, MN, WI
Recalling firm: Karben4 Brewing LLC, Madison, WI
FDA recall event 90233 · status Ongoing
FDA Enforcement Report → search event 90233
Reason (FDA): Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
Where it went (FDA): US Nationwide. Worldwide.
Recalling firm: Abbott Laboratories, Abbott Park, IL
FDA recall event 89629 · status Ongoing
FDA Enforcement Report → search event 89629
Reason (FDA): FDA was notified of cases of acute liver failure after consumption of Real Water
Where it went (FDA): Nationwide. Distributors located in WA, CA, AZ, NM, NV, RI, CO, MN, MO, IL, TN, AL, MS, GA, NY
Recalling firm: Real Water, Inc., Henderson, NV
FDA recall event 87552 · status Ongoing
FDA Enforcement Report → search event 87552
Reason (FDA): The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
Where it went (FDA): Product was shipped to the following states: GA, NC, SC & WV.
Recalling firm: Canteen Inc. dba MG Foods, Inc., Charlotte, NC
FDA recall event 87464 · status Ongoing
FDA Enforcement Report → search event 87464
Reason (FDA): Recall due to mold growth observed (Eurotium spp., Aspergillus niger, and Xeromyces bisporus).
Where it went (FDA): AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NH, NJ, NV, NY, OH, OR, PA, SC, SD, TN, TX, UT, VA, VI, WA, and WI. International consignees: Bermuda, Cambodia, South Africa, South Korea, Trinidad, and Tobago.
Recalling firm: Nurture Inc. dba Happy Family, New York, NY
FDA recall event 86606 · status Ongoing
FDA Enforcement Report → search event 86606
Reason (FDA): The firm received positive Environmental sampling results for Listeria monocytogenes.
Where it went (FDA): Product was shipped to the following states: MD, NC, PA, SC, & VA. North Carolina, Pennsylvania, South Carolina, and Virginia and to wholesalers in Maryland
Recalling firm: Freshouse Produce, Salisbury, NC
FDA recall event 86198 · status Ongoing
FDA Enforcement Report → search event 86198
Reason (FDA): Elevated histamine levels.
Where it went (FDA): Direct Distribution to FL, RI, CA, NJ
Recalling firm: Truong Phu Xanh Co.,, Quang Ngai, N/A
FDA recall event 84572 · status Ongoing
FDA Enforcement Report → search event 84572
Reason (FDA): The firm was informed by their customer that a random sample tested by the FDA test positive for norovirus.
Where it went (FDA): Distribution went to Wal-Mart and Save-A-Lot grocery stores in FL, GA, SC, NC, NY, TN, TX & WI.
Recalling firm: Riverside Foods Llc, Eagle, ID
FDA recall event 83016 · status Ongoing
FDA Enforcement Report → search event 83016
Reason (FDA): Products may be contaminated with Listeria monocytogenes.
Where it went (FDA): Product was shipped to North Carolina & South Carolina
Recalling firm: Grand Strand Sandwich Company,Inc., Longs, SC
FDA recall event 81900 · status Ongoing
FDA Enforcement Report → search event 81900
Reason (FDA): The firm was notified by their supplier that the vegetables used in the product were possibly contaminated with Listeria monocytogenes and Salmonella.
Where it went (FDA): Product was shipped to the following states: CT, FL, GA, MD, NY, OH & PA.
Recalling firm: J&J Snack Foods Handheld Corp, Holly Ridge, NC
FDA recall event 81432 · status Ongoing
FDA Enforcement Report → search event 81432
Reason (FDA): The firm was notified by their vendor that the product may be contaminated with Listeria monocytogenes.
Where it went (FDA): Product was shipped to the following states: CA, DE, GA, NC, NY, SC, VA & DC.
Recalling firm: Ladyfingers Catering, LLC, Raleigh, NC
FDA recall event 81175 · status Ongoing
FDA Enforcement Report → search event 81175
Reason (FDA): The firm was notified by a customer that the product test positive for Salmonella
Where it went (FDA): Product was shipped to AR & TN.
Recalling firm: Peanut Processors, Inc., Dublin, NC
FDA recall event 80599 · status Ongoing
FDA Enforcement Report → search event 80599
Reason (FDA): The product tested positive for Salmonella.
Where it went (FDA): All product was shipped to New York.
Recalling firm: MBG Marketing, Grand Junction, MI
FDA recall event 80600 · status Ongoing
FDA Enforcement Report → search event 80600
Reason (FDA): The firm was notified by their customer that the product test positive for Salmonella
Where it went (FDA): Product was shipped to the following states: AR, FL, IA, IN & NC
Recalling firm: Peanut Processors, Inc., Dublin, NC
FDA recall event 80391 · status Ongoing
FDA Enforcement Report → search event 80391
Reason (FDA): The firm was notified by the North Carolina Dept. of Agriculture that the product contains Salmonella.
Where it went (FDA): Product was distributed to NC & TN.
Recalling firm: Pious Lion, Fletcher, NC
FDA recall event 80151 · status Ongoing
FDA Enforcement Report → search event 80151
Reason (FDA): Shell eggs have the potential to be contaminated with Salmonella Braenderup.
Where it went (FDA): Direct consignees located in MS, NJ, GA, VA, FL, NH, NY, AL, NC, CT, MD, UT, & SC retail stores and restaurants via direct delivery.
Recalling firm: ROSE ACRE FARM, Seymour, IN
FDA recall event 79839 · status Ongoing
FDA Enforcement Report → search event 79839
Reason (FDA): Product contaminated with Listeria monocytogenes
Where it went (FDA): Distributed to FL, IL, KY, LA, NC.
Recalling firm: Global Garlic, Inc., Miami, FL
FDA recall event 77280 · status Ongoing
FDA Enforcement Report → search event 77280
Reason (FDA): FDA Environmental samples and finished product collected at the firm revealed the presence of Listeria monocytogenes. The firm is recalling the products due to the potential for Listeria contamination.
Where it went (FDA): Throughout Florida
Recalling firm: Gourmet Classic Salads, Inc., Lake Wales, FL
FDA recall event 76544 · status Ongoing
FDA Enforcement Report → search event 76544
Reason (FDA): Possible contamination with E. coli O157
Where it went (FDA): Product is distributed throughout Florida to child care programs and after school programs for children.
Recalling firm: Greater Miami Caterers, Inc., Miami, FL
FDA recall event 76786 · status Ongoing
FDA Enforcement Report → search event 76786
Reason (FDA): Sample of product collected by the State Department of Agriculture tested positive for Listeria Monocytogenes
Where it went (FDA): FL, GA, IL, IN, KS, KY, MA, MI, MO, MC, OH, PA, SC, TN, TX, UT
Recalling firm: MDS Foods Inc, Massillion, OH
FDA recall event 76441 · status Ongoing
FDA Enforcement Report → search event 76441
Reason (FDA): Contamination with Listeria monocytogenes
Where it went (FDA): Distributed throughout Florida
Recalling firm: Barberi International Inc., Miami, FL
FDA recall event 76336 · status Ongoing
FDA Enforcement Report → search event 76336
Reason (FDA): Product tested positive for Salmonella.
Where it went (FDA): FL, NY, & VA.
Recalling firm: Patel Shippers Inc, Miami, FL
FDA recall event 73996 · status Ongoing
FDA Enforcement Report → search event 73996
Reason (FDA): Undeclared Egg Allergen
Where it went (FDA): CA, AZ, NJ, MA, RI, CT, NY
Recalling firm: WFM Purchasing, LP, Austin, TX
FDA recall event 99874 · status Ongoing
FDA Enforcement Report → search event 99874
Reason (FDA): undeclared ingredients including but not limited to mustard
Where it went (FDA): Canada
Recalling firm: KRAFT HEINZ FOODS COMPANY, Chicago, IL
FDA recall event 99869 · status Ongoing
FDA Enforcement Report → search event 99869
Reason (FDA): Undeclared peanuts
Where it went (FDA): NY
Recalling firm: Quality Dairy Farms Inc., Boonville, NY
FDA recall event 99755 · status Ongoing
FDA Enforcement Report → search event 99755
Reason (FDA): Potential Wheat Kernel contamination.
Where it went (FDA): IA, IL, IN, KS, MN, OH PA, TX
Recalling firm: United Sugar Producers and Refiners, Minneapolis, MN
FDA recall event 99717 · status Ongoing
FDA Enforcement Report → search event 99717
Reason (FDA): Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no eggs in the product.
Where it went (FDA): Product was shipped to the following states: AL, FL, GA, IN, KY, MI, OH, TN, VA & WV.
Recalling firm: Best Friends Bakery, LLC, Connelly Springs, NC
FDA recall event 99803 · status Ongoing
FDA Enforcement Report → search event 99803
Reason (FDA): Undeclared milk and pecans
Where it went (FDA): IA, IL, IN, OH
Recalling firm: Ferrero USA, North Canton, OH
FDA recall event 99682 · status Ongoing
FDA Enforcement Report → search event 99682
Reason (FDA): Sesame is not declared in the ingredient statement but is declared in the statement of identity.
Where it went (FDA): New York.
Recalling firm: Prince Bakery Inc, Bronx, NY
FDA recall event 99646 · status Ongoing
FDA Enforcement Report → search event 99646
Reason (FDA): Label does not declare walnuts in English
Where it went (FDA): Domestic: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. Foreign: Canada, Switzerland, Colombia, Germany, Spain, United Kingdom, Japan, Norway, New Zealand, Saudi Arabia.
Recalling firm: Byron White Formulas, Inc., Santa Rosa, CA
FDA recall event 99629 · status Ongoing
FDA Enforcement Report → search event 99629
Reason (FDA): Labeling, wheat not listed as sub ingredient of chicken bouillon (minor ingredient), and soybean oil missing from ingredient list
Where it went (FDA): 8 wholesale and retail locations in IA, KY and IL
Recalling firm: Africando Foods LLC, Iowa City, IA
FDA recall event 99642 · status Ongoing
FDA Enforcement Report → search event 99642
Reason (FDA): Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio.
Where it went (FDA): Product is sold exclusively from the recalling firm's online website nationwide.
Recalling firm: L-Nutra Inc, Los Angeles, CA
FDA recall event 99675 · status Ongoing
FDA Enforcement Report → search event 99675
Reason (FDA): Undeclared Wheat.
Where it went (FDA): Product was sold in the U.S.
Recalling firm: EXOTIQUE FOODS CANADA, Etobicoke
FDA recall event 99636 · status Ongoing
FDA Enforcement Report → search event 99636
Reason (FDA): Product tested positive for undeclared milk allergen.
Where it went (FDA): 1 consignee in Canada
Recalling firm: Savor Seasonings LLC, Batavia, OH
FDA recall event 99644 · status Ongoing
FDA Enforcement Report → search event 99644
Reason (FDA): Undeclared Egg Allergen
Where it went (FDA): Texas
Recalling firm: Jaime's Foods ATX, LLC, Austin, TX
FDA recall event 99575 · status Ongoing
FDA Enforcement Report → search event 99575
Reason (FDA): Undeclared allergen (egg)
Where it went (FDA): IA, IL, OK, SD, TX
Recalling firm: Kerry, Inc, Beloit, WI
FDA recall event 99539 · status Ongoing
FDA Enforcement Report → search event 99539
Reason (FDA): Undeclared Red #40.
Where it went (FDA): Product is sold to independent manufacturer locations in Nevada, Arizona, Oregon, and California.12 locations total.
Recalling firm: FlavorsandColor.Com, Diamond Bar, CA
FDA recall event 99540 · status Ongoing
FDA Enforcement Report → search event 99540
Reason (FDA): Undeclared Egg
Where it went (FDA): Distributed to ID, FL, MI, MN, UT, OR, WA, OK, TX, NY, TN, IL, CA, KS, MA, NE, AZ, SC, MD, WI, GA, CO, WA, WV
Recalling firm: 529 COMMERCE, LLC, Parkland, FL
FDA recall event 99519 · status Ongoing
FDA Enforcement Report → search event 99519
Reason (FDA): Undeclared sulfites
Where it went (FDA): WI
Recalling firm: Elegant Foods, LLC, Madison, WI
FDA recall event 99572 · status Ongoing
FDA Enforcement Report → search event 99572
Reason (FDA): Undeclared milk from lactose.
Where it went (FDA): Product is exclusively distributed to two affiliated restaurants.
Recalling firm: Big Way Ca Inc, Pomona, CA
FDA recall event 99513 · status Ongoing
FDA Enforcement Report → search event 99513
Reason (FDA): The firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coconut).
Where it went (FDA): Product was shipped to the following states: DC, DE, GA, MD, NJ, NY, NC, PA, SC, & VA.
Recalling firm: Lidl US TRADING, Arlington, VA
FDA recall event 99493 · status Ongoing
FDA Enforcement Report → search event 99493
Reason (FDA): Undeclared Soy. The firm received complaints of sausage in the burritos. Upon review the firm discovered the sausage contains soy which is not listed on the label.
Where it went (FDA): Product was shipped to the following states: AL, GA, KY, NC, SC, TN, VA & WV.
Recalling firm: M.G. Foods, Inc., Charlotte, NC
FDA recall event 99458 · status Ongoing
FDA Enforcement Report → search event 99458
Reason (FDA): Undeclared peanuts.
Where it went (FDA): Domestic: AZ, CA, CO, HI, NJ, OR, TX, WA. Foreign: Not applicable.
Recalling firm: KHONG GUAN (HQ), Union City, CA
FDA recall event 99424 · status Ongoing
FDA Enforcement Report → search event 99424
Reason (FDA): Allergen missing from contains statement: fish
Where it went (FDA): NJ, CA
Recalling firm: Pack'n Fresh LLC, Grand Prairie, TX
FDA recall event 99460 · status Ongoing
FDA Enforcement Report → search event 99460
Reason (FDA): Undeclared milk.
Where it went (FDA): Domestic: CA, GA, IL, NJ, NY, TX Foreign: Canada, Australia
Recalling firm: Fayus Inc., Sacramento, CA
FDA recall event 99368 · status Ongoing
FDA Enforcement Report → search event 99368
Reason (FDA): Firm's finished product label does not declare the source of marine collagen which was determined to be fish.
Where it went (FDA): Product is distributed through TikTok exclusively. Presumably nationwide.
Recalling firm: Mellish Island Corp, San Dimas, CA
FDA recall event 99419 · status Ongoing
FDA Enforcement Report → search event 99419
Reason (FDA): Product label allergen "contains" statement does not include anchovy(fish)
Where it went (FDA): Product is shipped to a distributor's warehouse and distributed through online sales.
Recalling firm: JINA F&C, Gyeongju
FDA recall event 99358 · status Ongoing
FDA Enforcement Report → search event 99358
Reason (FDA): Undeclared Allergen (Fish)
Where it went (FDA): The adulterated product was distributed to the following states: NY, PA, CT, NC, TX, MD
Recalling firm: GELLERT GLOBAL GROUP, Elizabeth, NJ
FDA recall event 99357 · status Ongoing
FDA Enforcement Report → search event 99357
Reason (FDA): Undeclared peanuts
Where it went (FDA): Domestic: TX. Foreign: Not Applicable.
Recalling firm: Fayus Inc., Sacramento, CA
FDA recall event 99282 · status Ongoing
FDA Enforcement Report → search event 99282
Reason (FDA): Dietary supplement product Ocular Plus contains undeclared Yellow#5.
Where it went (FDA): Product was distributed to two local direct accounts. Both are local retail stores selling various vitamins and health products.
Recalling firm: Provision Health Corp. dba PH Labs, San Diego, CA
FDA recall event 99294 · status Ongoing
FDA Enforcement Report → search event 99294
Reason (FDA): Undeclared peanuts.
Where it went (FDA): Product was distributed to a single retail customer who further distributed product to their California located stores.
Recalling firm: Western Mixers Produce & Nuts, Inc., Ontario, CA
FDA recall event 99255 · status Ongoing
FDA Enforcement Report → search event 99255
Reason (FDA): Undeclared sodium tripolyphosphate (STTP)
Where it went (FDA): Domestic Distribution: CA Foreign Distribution: Not Applicable
Recalling firm: Shandong Ling Xian Food Co.,LTD, Rizhao, N/A
FDA recall event 99215 · status Ongoing
FDA Enforcement Report → search event 99215
Reason (FDA): Undeclared fish.
Where it went (FDA): Domestic: AK, AZ, CA, CO, FL, GA, HI, IL, MD, MA, NC, NJ, NV, NY, OR, TX, WA
Recalling firm: Azuma Foods International Inc USA, Hayward, CA
FDA recall event 99117 · status Ongoing
FDA Enforcement Report → search event 99117
Reason (FDA): Undeclared peanuts
Where it went (FDA): The product was distributed to WA.
Recalling firm: Bazzini LLC, Allentown, PA
FDA recall event 99097 · status Ongoing
FDA Enforcement Report → search event 99097
Reason (FDA): Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.
Where it went (FDA): Domestic: CA Foreign: Not applicable
Recalling firm: Boichik Bagels, Inc., Berkeley, CA
FDA recall event 99082 · status Ongoing
FDA Enforcement Report → search event 99082
Reason (FDA): Contains undeclared allergen (shrimp).
Where it went (FDA): AL, CT, DC, FL, GA, MA, MD, ME, MS, NC, NH, NJ, NY, PA, RI, SC, TN, VA
Recalling firm: Kettle Cuisine, LLC, Lynn, MA
FDA recall event 99038 · status Ongoing
FDA Enforcement Report → search event 99038
Reason (FDA): Undeclared Tree Nut Allergen
Where it went (FDA): Texas, California, Illinois, and New York. Two vessels in route to Korea.
Recalling firm: Wilco Peanut Co, Pleasanton, TX
FDA recall event 99057 · status Ongoing
FDA Enforcement Report → search event 99057
Reason (FDA): Undeclared Allergen (Soy)
Where it went (FDA): The recalled product was distributed to the following states: AL, AR, CO,GA, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, ND, NE, NM, OH, OK, SC, SD, TN, TX, WI, WV, WY
Recalling firm: Nutrisystem Inc, Fort Washington, PA
FDA recall event 99218 · status Ongoing
FDA Enforcement Report → search event 99218
Reason (FDA): Undeclared melatonin.
Where it went (FDA): Will be provided when available.
Recalling firm: Dkiru LLC, Sheridan, WY
FDA recall event 98984 · status Ongoing
FDA Enforcement Report → search event 98984
Reason (FDA): Sesame Seeds White were labeled as Curry Powder Sweet.
Where it went (FDA): WI
Recalling firm: J and J Bunting, Inc, Rogers, MN
FDA recall event 98965 · status Ongoing
FDA Enforcement Report → search event 98965
Reason (FDA): Undeclared walnuts
Where it went (FDA): U.S. Distribution: IL Foreign Distribution: Not Applicable
Recalling firm: The Brownie Baker Inc., Fresno, CA
FDA recall event 98857 · status Ongoing
FDA Enforcement Report → search event 98857
Reason (FDA): Contains undeclared allergens (cashews, milk, and soy).
Where it went (FDA): NY, NJ
Recalling firm: WE R NUTS, Port Washington, NY
FDA recall event 98807 · status Ongoing
FDA Enforcement Report → search event 98807
Reason (FDA): Undeclared Milk, Almonds, Soy, Sulfites.
Where it went (FDA): Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.
Recalling firm: Silver Moon LP dba Loard's Ice Cream, San Leandro, CA
FDA recall event 98782 · status Ongoing
FDA Enforcement Report → search event 98782
Reason (FDA): Undeclared milk.
Where it went (FDA): Domestic distribution: AK, AL, AR, AZ, CA, CO, FL, IA, ID, IL, IN, KS, LA, MI, MN, MO, MT, NE, NM, NV, OH, OK, OR, TN, TX, UT, VA, WA, WI. Foreign distribution: Canada, Japan.
Recalling firm: Marquez Brothers International, Inc., Fresno, CA
FDA recall event 98761 · status Ongoing
FDA Enforcement Report → search event 98761
Reason (FDA): Product contains undeclared milk.
Where it went (FDA): New York, New Jersey, Massachusetts, Virginia, Maryland, California, Washington, Texas
Recalling firm: HEYTEA USA INC, Santa Ana, CA
FDA recall event 98669 · status Ongoing
FDA Enforcement Report → search event 98669
Reason (FDA): Contains undeclared egg, soy, and hazelnut
Where it went (FDA): Alaska, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan, Minnesota, Mississippi, Montana, North Carolina, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia, & Wyoming
Recalling firm: Blueroot Health, Inc., Middletown, CT
FDA recall event 98663 · status Ongoing
FDA Enforcement Report → search event 98663
Reason (FDA): Label declares cream cheese but does not declare milk
Where it went (FDA): Distributed in CA, MA, NJ, NY, OR, TX, UT, VT.
Recalling firm: Riverence Provisions LLC, Buhl, ID
FDA recall event 98621 · status Ongoing
FDA Enforcement Report → search event 98621
Reason (FDA): Label does not specify type of tree nut contained in the product.
Where it went (FDA): DC, DE, GA, MD, NC, NJ, NY, PA, SC, VA
Recalling firm: Lidl US TRADING, Arlington, VA
FDA recall event 98584 · status Ongoing
FDA Enforcement Report → search event 98584
Reason (FDA): Undeclared Soy.
Where it went (FDA): Products distribute in FL
Recalling firm: South Florida Food, LLC, Hollywood, FL
FDA recall event 98547 · status Ongoing
FDA Enforcement Report → search event 98547
Reason (FDA): Label declares bovine colostrum but does not declare milk allergen.
Where it went (FDA): Product was distributed to: AR, FL, CO, CA, CT, HI, IN, IL, ID, IA, KS, KY, LA, OH, OK, OR, MA, MI, MN, MO, GA, NC, NE, ND, NY, PA, SC, TN, NJ, UT, TX, VA , WA, WV, WI, WY
Recalling firm: Pure Solutions, Inc., Tampa, FL
FDA recall event 98413 · status Ongoing
FDA Enforcement Report → search event 98413
Reason (FDA): Undeclared allergens (milk, soy, and peanut)
Where it went (FDA): AL, AZ, CA, FL, IA, KS, KY, MA, MD, MN, NC, NY, OH, PA, SD, TN, TX, VA, WA, WI
Recalling firm: Beacon Promotions Inc, Eagan, MN
FDA recall event 98336 · status Ongoing
FDA Enforcement Report → search event 98336
Reason (FDA): Undeclared Soy. Label did not include soy, which was used in product.
Where it went (FDA): Product was shipped to VA & WV.
Recalling firm: Ukrop's Homestyle Foods, LLC, Richmond, VA
FDA recall event 98155 · status Ongoing
FDA Enforcement Report → search event 98155
Reason (FDA): Undeclared Milk. Wrong product in container.
Where it went (FDA): All product was shipped to one distribution center in TX.
Recalling firm: Bakkavor, Charlotte, NC
FDA recall event 98121 · status Ongoing
FDA Enforcement Report → search event 98121
Reason (FDA): Undeclared wheat.
Where it went (FDA): U.S. distribution: CA Foreign distribution: N/A
Recalling firm: BHARAT BAZAR, Union City, CA
FDA recall event 98151 · status Ongoing
FDA Enforcement Report → search event 98151
Reason (FDA): elevated levels of chloramphenicol in frozen shrimp
Where it went (FDA): Product was shipped nationwide and distributed exclusively under the Member's Mark label.
Recalling firm: AZ Gems, Inc., Redlands, CA
FDA recall event 98160 · status Ongoing
FDA Enforcement Report → search event 98160
Reason (FDA): Undeclared caffeine
Where it went (FDA): FL, IA, MA, MD, MO, NC, NJ, NY, OH, WI
Recalling firm: Gimme Coffee, Inc., Ithaca, NY
FDA recall event 98042 · status Ongoing
FDA Enforcement Report → search event 98042
Reason (FDA): Undeclared sulfites
Where it went (FDA): The product was distributed to the following states: FL, GA, IA, NC
Recalling firm: Tai Phat Wholesalers, LLC, Capitol Heights, MD
FDA recall event 98179 · status Ongoing
FDA Enforcement Report → search event 98179
Reason (FDA): Undeclared Soy. The firm received positive test results for soy which is not listed on the label. The firm also noticed that the amount of boron in the product is listed as 250mg per serving instead of 250mcg per serving.
Where it went (FDA): Product was shipped to the following states: AL, AZ, CA, CO, FL, GA, IA, IL, KY, MA, MO, NY, OH, OK, PA, TX & VA.
Recalling firm: Avion Pharmaceuticals, LLC, Alpharetta, GA
FDA recall event 97893 · status Ongoing
FDA Enforcement Report → search event 97893
Reason (FDA): Undeclared Peanuts. The firm received two complaints that the product contains peanuts which are not listed in the ingredient statement.
Where it went (FDA): Product was shipped to one distribution center in IL.
Recalling firm: Jody's Inc., Norfolk, VA
FDA recall event 97829 · status Ongoing
FDA Enforcement Report → search event 97829
Reason (FDA): Contains undeclared cashews
Where it went (FDA): Connecticut, New York, New Jersey, and New Hampshire, Pennsylvania, Ohio, Nevada, Florida, and Wisconsin
Recalling firm: Nats Nuts LLC, Rochester, NY
FDA recall event 97828 · status Ongoing
FDA Enforcement Report → search event 97828
Reason (FDA): Undeclared allergen (wheat).
Where it went (FDA): U.S. Distribution: CA
Recalling firm: Gansu Zhaofeng Agricultural Development Co., Ltd., Longnan
FDA recall event 97645 · status Ongoing
FDA Enforcement Report → search event 97645
Reason (FDA): Undeclared Tree Nut. The firm discovered that Hazelnuts was not listed in the allergen statement
Where it went (FDA): Product was shipped to MA & NY.
Recalling firm: Severn Peanut Company LLC, Severn, NC
FDA recall event 97635 · status Ongoing
FDA Enforcement Report → search event 97635
Reason (FDA): May contained undeclared almond
Where it went (FDA): NY
Recalling firm: I C F Factory Inc, Mount Vernon, NY
FDA recall event 97514 · status Ongoing
FDA Enforcement Report → search event 97514
Reason (FDA): Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.
Where it went (FDA): Product is distributed to 30 US customers who receive and further process/package product prior to distribution.
Recalling firm: Herbal Creations USA, Ontario, CA
FDA recall event 98462 · status Ongoing
FDA Enforcement Report → search event 98462
Reason (FDA): Product label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: millet and flax
Where it went (FDA): NY, PA, NJ, TX, HI, LA, UT, CA, MD, ID, TN, IN, GA, MI, WA, ME, CT
Recalling firm: Bakers Authority LLC, Maspeth, NY
FDA recall event 97430 · status Ongoing
FDA Enforcement Report → search event 97430
Reason (FDA): Product label includes the ingredient CREAM but does not include Milk as the source.
Where it went (FDA): Nationwide distribution
Recalling firm: Tropicale Foods, LLC, Ontario, CA
FDA recall event 97346 · status Ongoing
FDA Enforcement Report → search event 97346
Reason (FDA): Undeclared milk from Contains statement.
Where it went (FDA): CA
Recalling firm: The Bonami Baking Company, Inc., Pittsburg, CA
FDA recall event 97347 · status Ongoing
FDA Enforcement Report → search event 97347
Reason (FDA): Undeclared egg.
Where it went (FDA): Product was shipped to the following states: AL, GA, NC, PA & SC.
Recalling firm: Hillside Orchard Farms Inc., Tiger, GA
FDA recall event 97298 · status Ongoing
FDA Enforcement Report → search event 97298
Reason (FDA): Undeclared allergens (Peanut) due to mispackaging
Where it went (FDA): The recalled product was distributed to the following states: AK,AL,AR,AZ,CA,CO,CT,DC,DE,FL,GA,HI,IA,ID,IL,IN,KS,KY,LA,MA,MD,ME,MI,MN,MO,MS,MT,NC,ND,NE,NH,NJ,NM,NV,NY,OH,OK,OR,PA,RI,SC,TN,TX,UT,VA,WA,WI,WV,WY
Recalling firm: Mondelez Global Llc, East Hanover, NJ
FDA recall event 97238 · status Ongoing
FDA Enforcement Report → search event 97238
Reason (FDA): Undeclared Sulfites in product
Where it went (FDA): NJ and NY
Recalling firm: NIRWANA FOODS LLC, Carteret, NJ
FDA recall event 97290 · status Ongoing
FDA Enforcement Report → search event 97290
Reason (FDA): Undeclared Milk.
Where it went (FDA): Product was shipped to the following states: IA, IL, IN, MN, ND, NE, NY, OH, SD, WI
Recalling firm: Homegrown Family Foods LLC, Conover, NC
FDA recall event 96863 · status Ongoing
FDA Enforcement Report → search event 96863
Reason (FDA): Undeclared allergens (milk and/or peanuts).
Where it went (FDA): CA, UT, WA
Recalling firm: Bondsforever, Inc dba Shastha Foods, San Jose, CA
FDA recall event 96846 · status Ongoing
FDA Enforcement Report → search event 96846
Reason (FDA): Contains undeclared almonds & undeclared sesame
Where it went (FDA): NY and New England
Recalling firm: Better Business...Better Foods, Inc., Milford, NH
FDA recall event 96758 · status Ongoing
FDA Enforcement Report → search event 96758
Reason (FDA): Undeclared Allergen (Soy)
Where it went (FDA): The adulterated product was distributed to the following states: CT, MA, IL, MD, NY, PA, TX, CA, IN, CO, NH, WI, GA, NJ, FL
Recalling firm: Dr. Praeger's Sensible Foods Inc., Elmwood Park, NJ
FDA recall event 96623 · status Ongoing
FDA Enforcement Report → search event 96623
Reason (FDA): Contains undeclared milk
Where it went (FDA): NY
Recalling firm: Optima Foods, Inc., Deer Park, NY
FDA recall event 96408 · status Ongoing
FDA Enforcement Report → search event 96408
Reason (FDA): Undeclared wheat. The firm was notified by their supplier that they failed to include the allergen "wheat" on the label.
Where it went (FDA): Product were shipped to retail stores in Georgia
Recalling firm: Grace Imports, Inc, Tucker, GA
FDA recall event 95311 · status Ongoing
FDA Enforcement Report → search event 95311
Reason (FDA): Undeclared whey (milk), wheat flour, almonds; no contains statement & no nutrition fact panel
Where it went (FDA): Firm distributes to local retail stores such as Walgreens.
Recalling firm: The Posh Bakery, Inc., Sacramento, CA
FDA recall event 95260 · status Ongoing
FDA Enforcement Report → search event 95260
Reason (FDA): Undeclared Fish Allergen
Where it went (FDA): Direct to consumer throughout the USA
Recalling firm: Quantum Fulfillment and Support, LLC, Cedar Creek, TX
FDA recall event 95443 · status Ongoing
FDA Enforcement Report → search event 95443
Reason (FDA): Undeclared allergen; peanuts
Where it went (FDA): CA, NV, WA, OR, ID, AK
Recalling firm: DSD Merchandisers, Inc., Livermore, CA
FDA recall event 94857 · status Ongoing
FDA Enforcement Report → search event 94857
Reason (FDA): Potential undeclared gluten product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.
Where it went (FDA): California and Oregon
Recalling firm: Best Express Foods, Inc., Stockton, CA
FDA recall event 95437 · status Ongoing
FDA Enforcement Report → search event 95437
Reason (FDA): Potential undeclared gluten product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.
Where it went (FDA): U.S. distribution to the following: CA, CO, AZ, WA, UT, TX, NJ, MD, IL, MI, MN, GA, FL Foreign distribution to the following: Canada
Recalling firm: Best Express Foods, Inc., Stockton, CA
FDA recall event 94897 · status Ongoing
FDA Enforcement Report → search event 94897
Reason (FDA): Product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.
Where it went (FDA): U.S. Distribution to WA and IL.
Recalling firm: Best Express Foods, Inc., Stockton, CA
FDA recall event 94677 · status Ongoing
FDA Enforcement Report → search event 94677
Reason (FDA): Product contains (allergen) undeclared egg.
Where it went (FDA): Product was shipped to NC and SC.
Recalling firm: County Road Seafood, LLC, Belhaven, NC
FDA recall event 94670 · status Ongoing
FDA Enforcement Report → search event 94670
Reason (FDA): Missing the declaration of sesame seeds from the "Contains" statement.
Where it went (FDA): U.S. distribution to the following: CA No foreign distribution.
Recalling firm: Della Fattoria, LLC, Petaluma, CA
FDA recall event 94615 · status Ongoing
FDA Enforcement Report → search event 94615
Reason (FDA): Undeclared allergen (milk)
Where it went (FDA): U.S. Distribution to the following states: CA, AK, IA, NY, TX, FL, WA, NJ, WA, VA, GA, TN, AZ, AL, NC. For foreign or government distribution.
Recalling firm: Sacramento Cookie Factory, Sacramento, CA
FDA recall event 94390 · status Ongoing
FDA Enforcement Report → search event 94390
Reason (FDA): During a contract inspection by the North Carolina Department of Agriculture, NCDA, informed the firm that the labeling does not list the common name of "milk".
Where it went (FDA): Product was shipped to one customer in VA
Recalling firm: Carolina CoPacking, LLC, Henderson, NC
FDA recall event 93603 · status Ongoing
FDA Enforcement Report → search event 93603
Reason (FDA): Undeclared soy
Where it went (FDA): Texas
Recalling firm: Somebody's Mother's Chocolate Sauce, Houston, TX
FDA recall event 92944 · status Ongoing
FDA Enforcement Report → search event 92944
Reason (FDA): The firm was notified that their labels do not list the allergens wheat and sesame.
Where it went (FDA): Product was shipped to one distributor in South Carolina.
Recalling firm: Saffron Inc., North Charleston, SC
FDA recall event 92663 · status Ongoing
FDA Enforcement Report → search event 92663
Reason (FDA): Undeclared Peanuts in bakery product.
Where it went (FDA): Product was shipped to the following states: DE, MD, NJ, PA, VA & WV.
Recalling firm: Flowers Foods (Corporate Offices), Thomasville, GA
FDA recall event 92396 · status Ongoing
FDA Enforcement Report → search event 92396
Reason (FDA): Undeclared milk
Where it went (FDA): Product was shipped to NC & SC.
Recalling firm: Washington Crab & Seafood Company, Inc., Washington, NC
FDA recall event 92122 · status Ongoing
FDA Enforcement Report → search event 92122
Reason (FDA): The firm was notified that a consumer had an allergic reaction to their product. The product did not list egg on the label.
Where it went (FDA): Product was shipped to the following states: CA, CO, FL, KY, NJ, OR & WA.
Recalling firm: SUMMIT NATURALS INC, Orlando, FL
FDA recall event 92172 · status Ongoing
FDA Enforcement Report → search event 92172
Reason (FDA): Colostrum is declared but label does not declare milk.
Where it went (FDA): Distributed in CA, FL, NJ, and NY.
Recalling firm: FLP LLC, Tempe, AZ
FDA recall event 92087 · status Ongoing
FDA Enforcement Report → search event 92087
Reason (FDA): During an internal inspection the firm discovered that several products may contain soy lecithin which is not declared on the labels.
Where it went (FDA): Product was shipped to the following states: AL, AZ, AR, CA, CO, CT, DE, DC, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, PR?, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI & WY. Product was also shipped to: Canada & Mexico.
Recalling firm: Flowers Foods (Corporate Offices), Thomasville, GA
FDA recall event 90975 · status Ongoing
FDA Enforcement Report → search event 90975
Reason (FDA): The firm stated that pecan pieces were packaged in pouches labeled as walnuts.
Where it went (FDA): Product was shipped to distribution centers in North Carolina and Florida.
Recalling firm: South Georgia Pecan Company, Valdosta, GA
FDA recall event 90770 · status Ongoing
FDA Enforcement Report → search event 90770
Reason (FDA): Undeclared soy, Red #40 & sulfites
Where it went (FDA): Product was shipped to the following states: GA, NC & SC.
Recalling firm: Select Bakery Inc., Rockwell, NC
FDA recall event 90485 · status Ongoing
FDA Enforcement Report → search event 90485
Reason (FDA): The label does not identify whey protein concentrate, contained in the stabilizer, as Milk.
Where it went (FDA): WI
Recalling firm: Elegant Foods, LLC, Madison, WI
FDA recall event 90020 · status Ongoing
FDA Enforcement Report → search event 90020
Reason (FDA): Undeclared soy in Tartar sauce. Ingredients statement declares soybean oil.
Where it went (FDA): Distributors in two states: OR and SC.
Recalling firm: Beaverton Foods Inc, Hillsboro, OR
FDA recall event 89273 · status Ongoing
FDA Enforcement Report → search event 89273
Reason (FDA): Undeclared milk
Where it went (FDA): Product was shipped to the following states: AZ, CA, CO, NM, NV, and WY.
Recalling firm: Flowers Foods (Corporate Offices), Thomasville, GA
FDA recall event 89239 · status Ongoing
FDA Enforcement Report → search event 89239
Reason (FDA): Undeclared soy allergen in frozen pizza
Where it went (FDA): Product was distributed to a distributor in OR who further distributed to 13 New Seasons Market locations in OR and WA.
Recalling firm: Mi Piace LLC, Portland, OR
FDA recall event 88993 · status Ongoing
FDA Enforcement Report → search event 88993
Reason (FDA): The firm was notified during an inspection by the State that the product contains undeclared soy.
Where it went (FDA): The product was shipped to the following states: AL, AR, AZ, CA, CO, FL, GA, IL, IN, KS, KY, MA, MD, MI, MN, NC, NE, NJ, NV, NY, OH, PA, SC, TN, TX, VA, VT & WV. Product was also shipped to the United Kingdom
Recalling firm: Molly and Me Pecans, Holly Hill, SC
FDA recall event 88279 · status Ongoing
FDA Enforcement Report → search event 88279
Reason (FDA): During an inspection by the FDA the firm was notified by FDA that the product contains undeclared milk, wheat & soy.
Where it went (FDA): Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, IL, IN, KY, LA, MA, MD, ME, MI, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV & WY.
Recalling firm: Hi Tech Pharmaceuticals, Norcross, GA
FDA recall event 87655 · status Ongoing
FDA Enforcement Report → search event 87655
Reason (FDA): Product may contain undeclared almonds.
Where it went (FDA): NV, IL, MD, NJ, TX, IL, PA, OR, IA
Recalling firm: HU PRODUCTS, New York, NY
FDA recall event 87468 · status Ongoing
FDA Enforcement Report → search event 87468
Reason (FDA): The firm was notified by the South Carolina Dept. of Agriculture that the product contains soy which is not included on the label.
Where it went (FDA): Product was shipped to the following states: GA & SC.
Recalling firm: Sweeteeth Chocolate LLC, Hanahan, SC
FDA recall event 86143 · status Ongoing
FDA Enforcement Report → search event 86143
Reason (FDA): The firm was notified by the FDA that they failed to included a shellfish allergen on their ingredient panel.
Where it went (FDA): Product was shipped to the following states: AZ, CA, FL, GA, IA, MI, MN, NC, NM, NV, NY, OH,PA, TN, TX, VA & WA.
Recalling firm: Absorb Health LLC, Supply, NC
FDA recall event 85242 · status Ongoing
FDA Enforcement Report → search event 85242
Reason (FDA): The firm was notified that the product contains undeclared soy.
Where it went (FDA): Product was shipped to their distributor in NC
Recalling firm: Harris Teeter Supermarkets, LLC dba Hunter Farms, High Point, NC
FDA recall event 84941 · status Ongoing
FDA Enforcement Report → search event 84941
Reason (FDA): The product contains undeclared sulfites.
Where it went (FDA): Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DC, DE, FL GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NH, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI & WY.
Recalling firm: TFI Holding dba Grey Ghost Bakery, Charleston, SC
FDA recall event 84523 · status Ongoing
FDA Enforcement Report → search event 84523
Reason (FDA): The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.
Where it went (FDA): Product was shipped to AL, NC & VA.
Recalling firm: Harris Teeter Supermarkets, LLC dba Hunter Farms, High Point, NC
FDA recall event 84085 · status Ongoing
FDA Enforcement Report → search event 84085
Reason (FDA): The product ingredient statement does not list walnuts in the product.
Where it went (FDA): Product was distributed to the following states: AL, FL, GA, IN, KY, LA, MD, MN, MS, NC, NY, OH, PA, SC, TN & VA.
Recalling firm: Gullah Gourmet, Inc., Charleston, SC
FDA recall event 83936 · status Ongoing
FDA Enforcement Report → search event 83936
Reason (FDA): Package did not contain Vanilla Bean Ice Cream but Cotton Candy Ice Cream, which contains soy lecithin that is not listed on the Vanilla Bean label.
Where it went (FDA): All product was shipped to one distributor in Pennsylvania
Recalling firm: Harris Teeter Supermarkets, LLC dba Hunter Farms, High Point, NC
FDA recall event 81593 · status Ongoing
FDA Enforcement Report → search event 81593
Reason (FDA): During a label check the firm noticed that the product was shipped with the incorrect label. The label is missing the following ingredients: Soybean Oil, Onion Powder & EDTA.
Where it went (FDA): Product was shipped to the following states: CA, GA, IL, LA, MA, MI, NC, NJ, OH, PA & TN.
Recalling firm: Diamond Crystal Brands, Inc., Savannah, GA
FDA recall event 81279 · status Ongoing
FDA Enforcement Report → search event 81279
Reason (FDA): During a South Carolina State Department inspection the firm was notified that the label did not list wheat as an ingredient.
Where it went (FDA): Product was shipped to the following states: CT & UT.
Recalling firm: Heritage Short Bread, Inc., Hilton Head Island, SC
FDA recall event 80026 · status Ongoing
FDA Enforcement Report → search event 80026
Reason (FDA): Canned spinach is being recalled due to the potential to contain boiled peanuts instead of spinach.
Where it went (FDA): Florida, Georgia, Iowa, Illinois, Indiana, Kentucky, Michigan, Minnesota, North Carolina, Ohio, South Carolina, South Dakota, Tennessee, Virginia, Wisconsin, and West Virginia.
Recalling firm: Mccall Farms Inc, Effingham, SC
FDA recall event 79912 · status Ongoing
FDA Enforcement Report → search event 79912
Reason (FDA): Undeclared soy and wheat ingredients
Where it went (FDA): Nationwide (U.S.): SC, FL, WA, KS, GA, NC, TX, TN, OH, MT, & AL
Recalling firm: Piggie Park Enterprises Inc, West Columbia, SC
FDA recall event 79473 · status Ongoing
FDA Enforcement Report → search event 79473
Reason (FDA): Snyder's Lance is voluntarily recalling 6.5 oz. Emerald brand walnuts due to the presence of undeclared peanuts, almonds, cashews, and pecans.
Where it went (FDA): U.S. - Nationwide
Recalling firm: Snyder's-Lance Inc., Charlotte, NC
FDA recall event 79311 · status Ongoing
FDA Enforcement Report → search event 79311
Reason (FDA): Cheesecake has incorrect rear label. The rear label is for Pumpkin Swirl Cheesecake which lacks peanut allergen declaration.
Where it went (FDA): Distributed in Florida and Georgia
Recalling firm: The Father's Table, LLC, Sanford, FL
FDA recall event 77225 · status Ongoing
FDA Enforcement Report → search event 77225
Reason (FDA): Undeclared Allergen: Milk
Where it went (FDA): CA and IL
Recalling firm: Bak EZ, Norcross, GA
FDA recall event 76703 · status Ongoing
FDA Enforcement Report → search event 76703
Reason (FDA): The Egg Bagel flavor lacks declaration of Yellow 5 on its label.
Where it went (FDA): Distributed only within Florida.
Recalling firm: O'Pelle Enterprises, Inc., Pompano Beach, FL
FDA recall event 75912 · status Ongoing
FDA Enforcement Report → search event 75912
Reason (FDA): Initiated by the Florida Department of Agriculture and Consumer Services due to undeclared sulfites on the finished product label.
Where it went (FDA): FLORIDA
Recalling firm: Commerce International Inc., Orlando, FL
FDA recall event 74984 · status Ongoing
FDA Enforcement Report → search event 74984
Reason (FDA): Initiated by the Florida Department of Agriculture and Consumer Services due to undeclared sulfites on the finished product label.
Where it went (FDA): FL, GA, NC, and SC.
Recalling firm: Commerce International Inc., Orlando, FL
FDA recall event 75605 · status Ongoing
FDA Enforcement Report → search event 75605
Reason (FDA): Undeclared allergen; Peanut Protein
Where it went (FDA): GA & NC
Recalling firm: Dessert Innovations II Candy Divison, Atlanta, GA
FDA recall event 74014 · status Ongoing
FDA Enforcement Report → search event 74014
Reason (FDA): Products contain undeclared milk on finished product labeling
Where it went (FDA): Product distributed nationwide an internationally to the following countries: Egypt, Bermuda, and United Arab Emirates
Recalling firm: Ouhlala Gourmet Llc, Coral Gables, FL
FDA recall event 73670 · status Ongoing
FDA Enforcement Report → search event 73670
Reason (FDA): Product contains undeclared Allergen; Almonds.
Where it went (FDA): AZ, CO, CT, DE, GA, IA, IN, MA, MD, MN, MO, NC, NH, NY, PA, TX and WI.
Recalling firm: Talenti Gelato, Marietta, GA
FDA recall event 66252 · status Ongoing
FDA Enforcement Report → search event 66252
Reason (FDA): Product contains undeclared Allergen; Pecans.
Where it went (FDA): Alaska, CT, ID, IL, IN, MD, MA, MT, NH, NJ, NY, NC, OH, PA, TN, VA, WA and WI.
Recalling firm: Talenti Gelato, Marietta, GA
FDA recall event 65592 · status Ongoing
FDA Enforcement Report → search event 65592
Reason (FDA): Product may contain foreign material: small stones and other hard objects.
Where it went (FDA): Product was distributed nationwide.
Recalling firm: WWF Operating Company, Louisville, CO
FDA recall event 99884 · status Ongoing
FDA Enforcement Report → search event 99884
Reason (FDA): Potential contamination with pesticides.
Where it went (FDA): Domestic: CA. Foreign: Not Applicable.
Recalling firm: Kwok Shing, Inc., San Francisco, CA
FDA recall event 99859 · status Ongoing
FDA Enforcement Report → search event 99859
Reason (FDA): Unapproved dye Ponceau 4R
Where it went (FDA): AZ, NY, CA, FL, GA, IL, MA, MN, NC, NJ, OH, PA, NY, TN, TX, VA
Recalling firm: Tiffany Food Corp, Brooklyn, NY
FDA recall event 99815 · status Ongoing
FDA Enforcement Report → search event 99815
Reason (FDA): Foreign object: products may contain glass pieces
Where it went (FDA): The adulterated product was distributed to the following States: AL, AR, AZ, CA,CO,CT, FL,GA, IA,ID, IL, KS, LA, MA,MD,MI, MN,MO, NC, ND, NH, NJ, NV, NY, OH, PA, PR, TN TX, UT, VA, VI, WA, and WI.
Recalling firm: Dreyer's Grand Ice Cream Inc., Laurel, MD
FDA recall event 99716 · status Ongoing
FDA Enforcement Report → search event 99716
Reason (FDA): Potential foreign object contamination: rubber pieces
Where it went (FDA): MA, ME, VT
Recalling firm: Gifford's Dairy, Inc., Skowhegan, ME
FDA recall event 99663 · status Ongoing
FDA Enforcement Report → search event 99663
Reason (FDA): Foreign object: May contain metal pieces
Where it went (FDA): Distributed in WA only.
Recalling firm: Grand Central Bakery - Oregon Inc. dba Grand Central Bakery, Inc., Portland, OR
FDA recall event 99639 · status Ongoing
FDA Enforcement Report → search event 99639
Reason (FDA): Product may have been improperly pasteurized.
Where it went (FDA): NJ
Recalling firm: UPSTATE NIAGARA COOPERATIVE, Lancaster, NY
FDA recall event 99619 · status Ongoing
FDA Enforcement Report → search event 99619
Reason (FDA): Product has high patulin levels
Where it went (FDA): The recalled product was distributed to the State of PA.
Recalling firm: WEIS MARKETS, INC., Sunbury, PA
FDA recall event 99638 · status Ongoing
FDA Enforcement Report → search event 99638
Reason (FDA): The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.
Where it went (FDA): The adulterated product was distributed to the following states: VA, NY, NJ, MI
Recalling firm: EURO FOODS GROUP USA NJ INC, Totowa, NJ
FDA recall event 99684 · status Ongoing
FDA Enforcement Report → search event 99684
Reason (FDA): Foreign object: metal fragments
Where it went (FDA): Product was shipped to the following states: KY, NC, VA & WVA.
Recalling firm: Ukrop's Homestyle Foods LLC, North Chesterfield, VA
FDA recall event 99548 · status Ongoing
FDA Enforcement Report → search event 99548
Reason (FDA): Flexible food pouch may release thin plastic strips into food.
Where it went (FDA): only in OR.
Recalling firm: CHEER PACK, West Bridgewater, MA
FDA recall event 99444 · status Ongoing
FDA Enforcement Report → search event 99444
Reason (FDA): Possible foreign object (thin, soft plastic strands).
Where it went (FDA): Distributed in AL, AZ, CA, CO, GA, IA, IL, IN, KS, MI, MN, NC, NJ, NY, OH, OR, PA, SC, TN, TX, VA, WA, and WI.
Recalling firm: PT Organics Limited, Lake Oswego, OR
FDA recall event 99448 · status Ongoing
FDA Enforcement Report → search event 99448
Reason (FDA): Foreign Manufacturer label contains Undeclared allergen ingredients Wheat, Soy, Sesame, Yellow #5 and Blue #1 in Frozen Flounder Products.
Where it went (FDA): CA, NJ
Recalling firm: Eunha Fisheries Co., LTD, Gangseo
FDA recall event 99351 · status Ongoing
FDA Enforcement Report → search event 99351
Reason (FDA): Potential foreign material (glass)
Where it went (FDA): AR, CA, FL, GA, IN, LA, ME, MO, NM, NY, OH, OK, PA, SC, TN, TX, VA, WA, WY
Recalling firm: General Mills James Ford Bell Technical Center, Golden Valley, MN
FDA recall event 99293 · status Ongoing
FDA Enforcement Report → search event 99293
Reason (FDA): Foreign material: small metal pieces
Where it went (FDA): Product was distributed to PA, TX, IN, FL
Recalling firm: Wondermade LLC, Sanford, FL
FDA recall event 99235 · status Ongoing
FDA Enforcement Report → search event 99235
Reason (FDA): Product may contain metal fragments.
Where it went (FDA): The adulterated product was distributed to the following states : NY, NJ, OH, PA
Recalling firm: W.Y. Industries, Inc., North Bergen, NJ
FDA recall event 99238 · status Ongoing
FDA Enforcement Report → search event 99238
Reason (FDA): The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3.
Where it went (FDA): The adulterated product was distributed to the following States: NC, VA, PA, NJ, NY, SC, FL
Recalling firm: Wise Foods Inc, Berwick, PA
FDA recall event 99124 · status Ongoing
FDA Enforcement Report → search event 99124
Reason (FDA): Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
Where it went (FDA): Product was shipped to the following states: AK, AL, AR, AZ, CA, CO, CT, Washington DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV. Product was also shipped to Canada & Australia.
Recalling firm: Nutricia North America, White Plains, NY
FDA recall event 99074 · status Ongoing
FDA Enforcement Report → search event 99074
Reason (FDA): Foreign material (Glass) was found in the product.
Where it went (FDA): The adulterated product was sent to the following states. NY,PA,NJ,CT,
Recalling firm: GELLERT GLOBAL GROUP, Elizabeth, NJ
FDA recall event 99055 · status Ongoing
FDA Enforcement Report → search event 99055
Reason (FDA): Potential contamination with lead.
Where it went (FDA): Domestic: AK, AR, CA, CO, FL, IA, ID, IL, IN, KS, KY, LA, MI, MN, MO, MS, MT, NE, NM, OR, SC, TX, UT, WA, WI. Foreign: Not applicable.
Recalling firm: U.S. Tov, Inc. dba U.S. Trading Company, Hayward, CA
FDA recall event 99017 · status Ongoing
FDA Enforcement Report → search event 99017
Reason (FDA): Potential contamination with foreign objects (metal pieces).
Where it went (FDA): Domestic: CA, CO, AZ, CT, FL, GA, IA, IL, IN, MD, NJ, OR, PA, SC, TX, WA, WI. Foreign: Not Applicable.
Recalling firm: Straus Family Creamery, Petaluma, CA
FDA recall event 98982 · status Ongoing
FDA Enforcement Report → search event 98982
Reason (FDA): Foreign object: black particulate matter
Where it went (FDA): Distributed to MO, IL, NJ, NY, TX, FL, PR, MA, OK, VA, MN, IA, OH, GA, WI, WA, CA, IN, NC, CO, TN, MA, MO, WV, AZ, DE
Recalling firm: Llorens Pharmaceuticals International Division, Inc., Miami, FL
FDA recall event 98958 · status Ongoing
FDA Enforcement Report → search event 98958
Reason (FDA): The product contains unapproved colors chlorophyll E140 and E141.
Where it went (FDA): USA
Recalling firm: MID DOLCIARIA SRL, Belpasso
FDA recall event 98926 · status Ongoing
FDA Enforcement Report → search event 98926
Reason (FDA): Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).
Where it went (FDA): NY
Recalling firm: Guangdong Zonegoing Food Co., LTD, Huizhou
FDA recall event 98757 · status Ongoing
FDA Enforcement Report → search event 98757
Reason (FDA): Foreign object (stainless steel dust/flakes or shreds of plastic)
Where it went (FDA): Retail locations in FL, GA, and SD Internet sales Nationwide
Recalling firm: Dakota Honey Company, Winner, SD
FDA recall event 98743 · status Ongoing
FDA Enforcement Report → search event 98743
Reason (FDA): Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.
Where it went (FDA): Texas
Recalling firm: Walker Honey Co, Rogers, TX
FDA recall event 98726 · status Ongoing
FDA Enforcement Report → search event 98726
Reason (FDA): The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
Where it went (FDA): The firm markets their products online via their website addallxr.com
Recalling firm: ZMB Enterprises, Carlsbad, CA
FDA recall event 98691 · status Ongoing
FDA Enforcement Report → search event 98691
Reason (FDA): Potential contamination with pesticides, haloxyfop and thiamethoxam
Where it went (FDA): U.S. Distribution: CA, CO, HI, MO, TX, VT, WA. Foreign Distribution: None.
Recalling firm: Falcon Trading Co., Inc., Royal Oaks, CA
FDA recall event 98662 · status Ongoing
FDA Enforcement Report → search event 98662
Reason (FDA): FDA analysis revealed the presence of undeclared sildenafil and Tadalafil
Where it went (FDA): New Jersey
Recalling firm: Pure Vitamins and Natural Supplements, LLC, Tampa, FL
FDA recall event 98592 · status Ongoing
FDA Enforcement Report → search event 98592
Reason (FDA): Product does not meet label claim for Vitamin E.
Where it went (FDA): Product was distributed to two domestic consignees who further distribute nationwide.
Recalling firm: Sato Pharmaceutical Inc., Torrance, CA
FDA recall event 98948 · status Ongoing
FDA Enforcement Report → search event 98948
Reason (FDA): Foreign object (glass) found inside sealed container of finished product.
Where it went (FDA): Distribution was to two consignees who have a total of 53 retail locations nationwide.
Recalling firm: Western Mixers Produce & Nuts, Inc., Ontario, CA
FDA recall event 98589 · status Ongoing
FDA Enforcement Report → search event 98589
Reason (FDA): Foreign objects are glass varying in size from 1‑3cm long and 2‑4mm wide.
Where it went (FDA): Distributed in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, and WY.
Recalling firm: Ajinomoto Foods North America Inc., Ontario, CA
FDA recall event 98535 · status Ongoing
FDA Enforcement Report → search event 98535
Reason (FDA): No process authority
Where it went (FDA): Product was shipped to one facility in GA.
Recalling firm: BlueFrog Foods, Austell, GA
FDA recall event 98515 · status Ongoing
FDA Enforcement Report → search event 98515
Reason (FDA): Water was bottled under insanitary conditions.
Where it went (FDA): IL, WI
Recalling firm: Valley Springs Artesian Gold, LLC, Portage, WI
FDA recall event 98410 · status Ongoing
FDA Enforcement Report → search event 98410
Reason (FDA): Potential contamination with patulin.
Where it went (FDA): U.S. Consignees: IL
Recalling firm: IF Holding II, LLC, Sanger, CA
FDA recall event 98337 · status Ongoing
FDA Enforcement Report → search event 98337
Reason (FDA): Uneviscerated Fish
Where it went (FDA): AZ, CA, FL, GA, HI, ID, MA, MD, MO, NJ, NV, NY, OH, OK, PA, VA, WA, WI
Recalling firm: Prime Food Processing LLC., Brooklyn, NY
FDA recall event 98390 · status Ongoing
FDA Enforcement Report → search event 98390
Reason (FDA): Undeclared tadalafil
Where it went (FDA): The product was distributed nationwide through third-party e-commerce marketplace: Amazon.com
Recalling firm: AKKARCO LLC, Lorton, VA
FDA recall event 98392 · status Ongoing
FDA Enforcement Report → search event 98392
Reason (FDA): Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.
Where it went (FDA): Nationwide and Puerto Rico
Recalling firm: Gerber Products Company dba Nestle Infant Nutrition, Arlington, VA
FDA recall event 98350 · status Ongoing
FDA Enforcement Report → search event 98350
Reason (FDA): Metal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by one of their ingredient suppliers.
Where it went (FDA): Product was shipped to the following states: AZ, CA, CT, FL, IL, MI, NC, NJ, TX & VA.
Recalling firm: Bakkavor, Charlotte, NC
FDA recall event 98311 · status Ongoing
FDA Enforcement Report → search event 98311
Reason (FDA): FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
Where it went (FDA): The recalled product was distributed to customers nationwide from April 2022 until December 8, 2025
Recalling firm: Modern Warrior Life, LLC, Scottsdale, AZ
FDA recall event 98304 · status Ongoing
FDA Enforcement Report → search event 98304
Reason (FDA): Glass in Pickles. The firm received complaints of glass found in the product.
Where it went (FDA): Product was shipped to warehouses in ME & NY.
Recalling firm: Mount Olive Pickle Company, Inc., Mount Olive, NC
FDA recall event 98259 · status Ongoing
FDA Enforcement Report → search event 98259
Reason (FDA): Potential exposure of rodents and rodent activity in the distribution center.
Where it went (FDA): IN, MN, ND
Recalling firm: GOLD STAR DISTRIBUTION INC, Minneapolis, MN
FDA recall event 98223 · status Ongoing
FDA Enforcement Report → search event 98223
Reason (FDA): Potential contamination with leachable lead.
Where it went (FDA): U.S. Distribution: CA, CO
Recalling firm: Lotus Mom Corporation dba Indian Kitchen Mart, San Jose, CA
FDA recall event 98092 · status Ongoing
FDA Enforcement Report → search event 98092
Reason (FDA): Potential contamination with heavy metal (lead).
Where it went (FDA): U.S. Distribution: CA, NV, WA
Recalling firm: VENZU TRADERS LLC, Fremont, CA
FDA recall event 98090 · status Ongoing
FDA Enforcement Report → search event 98090
Reason (FDA): Potential contamination due to leachable lead.
Where it went (FDA): U.S. Distribution: CA
Recalling firm: Santos Agency Inc., San Leandro, CA
FDA recall event 97984 · status Ongoing
FDA Enforcement Report → search event 97984
Reason (FDA): Unapproved color (carmoisine).
Where it went (FDA): U.S. distribution: CA Foreign distribution: None
Recalling firm: Mangalm LLC, Newark, CA
FDA recall event 97995 · status Ongoing
FDA Enforcement Report → search event 97995
Reason (FDA): Potential contamination due to leachable lead.
Where it went (FDA): U.S. Distribution: CA
Recalling firm: INDIAN COOKWARE AND APPLIANCE LLC, San Jose, CA
FDA recall event 97962 · status Ongoing
FDA Enforcement Report → search event 97962
Reason (FDA): Potential contamination due to leachable lead.
Where it went (FDA): U.S. Distribution: CA, WA
Recalling firm: India's Fine Foods, Inc., West Sacramento, CA
FDA recall event 97898 · status Ongoing
FDA Enforcement Report → search event 97898
Reason (FDA): Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Where it went (FDA): Product was shipped to the following states: AL, AZ, CA, FL, HI, IA, IL, IN, MA, MI, MO, MS, NC, NJ, NY, OR, PA, PR, RI, TN, TX, UT, WA, WI & WV.
Recalling firm: Winder Laboratories, LLC, Winder, GA
FDA recall event 97884 · status Ongoing
FDA Enforcement Report → search event 97884
Reason (FDA): contains high levels of lead (10.7 mg/kg)
Where it went (FDA): MA
Recalling firm: Good Way Trading Group Inc, Maspeth, NY
FDA recall event 97865 · status Ongoing
FDA Enforcement Report → search event 97865
Reason (FDA): Product found to contain leachable lead levels.
Where it went (FDA): AL, AR, AZ, CA, CO, FL, GA, IL, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NV, NY, OH, OK, PA, RI, SC, SD, TN, TX, UT, VT, WA, WV, Puerto Rico and Quebec City , Canada
Recalling firm: Town Food Service Equip Co Inc, Brooklyn, NY
FDA recall event 98033 · status Ongoing
FDA Enforcement Report → search event 98033
Reason (FDA): Elevated levels of lead in Cinnamon powder.
Where it went (FDA): Product was distributed to retail locations across the country.
Recalling firm: Haitai, Inc., Cerritos, CA
FDA recall event 97836 · status Ongoing
FDA Enforcement Report → search event 97836
Reason (FDA): potential for metal in product
Where it went (FDA): These products were distributed in the United States. Consumers may have purchased impacted product via retail stores and online retail, including but not limited to: Albertson s, CVS, Food Lion, H-E-B, Hungryroot, Ingles Markets, Kroger, Stew Leonard s, and Target.
Recalling firm: Georgia Nut Co, Skokie, IL
FDA recall event 97701 · status Ongoing
FDA Enforcement Report → search event 97701
Reason (FDA): Shrimp may be contaminated with Cesium-137 (Cs-137).
Where it went (FDA): Nationwide.
Recalling firm: Admiralty Island Fisheries Inc dba AquaStar (USA) Corp., Seattle, WA
FDA recall event 97667 · status Ongoing
FDA Enforcement Report → search event 97667
Reason (FDA): Potential contamination with heavy metal (Lead).
Where it went (FDA): U.S. States: AZ, CA, CO, CT, FL, GA, HI, ID, IN, KY, LA, MA, MD, MI, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, PA, RI, TN, TX, UT, VA, WA, WI U.S. Territories: Puerto Rico
Recalling firm: Sprout Organics Inc., San Rafael, CA
FDA recall event 97622 · status Ongoing
FDA Enforcement Report → search event 97622
Reason (FDA): Elevated levels of lead.
Where it went (FDA): a total of 11 retail and 1 wholesale customers across two states (California and Michigan)
Recalling firm: EUREKA INC, Pomona, CA
FDA recall event 97767 · status Ongoing
FDA Enforcement Report → search event 97767
Reason (FDA): Product may be contaminated with Cesium-137 (Cs-137).
Where it went (FDA): The affected AquaStar brand Cocktail Shrimp, 4oz. shrimp/2oz. cocktail sauce (net wt. 6oz), was sold at WALMART stores in AK, AL, AR, CO, GA, IA, ID, IL, IN, KS, KY, LA, MI, MN, MO, MS, MT, ND, NE, OH, OK, OR, SD, TN, TX, WA, and WI between 7/31/25 and 8/16/25. The affected KROGER Mercado brand shrimp 2lb. was sold at Baker's, Gerbes, Jay C, Kroger, Mariano s, Metro Market, Pay Less Supermarkets, and Pick n Save in AL, AR, GA, IL, IN, KS, KY, MI, MO, MS, NE, OH, SC, TN, VA, WI, WV between 7/24/25 and 8/11/25.
Recalling firm: Admiralty Island Fisheries Inc dba AquaStar (USA) Corp., Seattle, WA
FDA recall event 97493 · status Ongoing
FDA Enforcement Report → search event 97493
Reason (FDA): Potential contamination with foreign objects.
Where it went (FDA): CA, UT
Recalling firm: Domino Foods Inc, West Palm Beach, FL
FDA recall event 97462 · status Ongoing
FDA Enforcement Report → search event 97462
Reason (FDA): Potential contamination with foreign materials.
Where it went (FDA): TX
Recalling firm: Valley Fine Foods Co., Inc, Benicia, CA
FDA recall event 96733 · status Ongoing
FDA Enforcement Report → search event 96733
Reason (FDA): Potential contamination with foreign objects (metal)
Where it went (FDA): CA, IL, TX
Recalling firm: Pacific Meridian Group, LLC, Oakland, CA
FDA recall event 96641 · status Ongoing
FDA Enforcement Report → search event 96641
Reason (FDA): Elevated levels of Sulfites in Dried Longan Pulp
Where it went (FDA): Product was distributed to customers in CA, TX, WA, OR, AZ, FL, NV
Recalling firm: Growland Inc, Chino, CA
FDA recall event 96264 · status Ongoing
FDA Enforcement Report → search event 96264
Reason (FDA): Potential contamination with foreign objects.
Where it went (FDA): KY, MI, OH, PA.
Recalling firm: Pacific Coast Producers, Lodi, CA
FDA recall event 96005 · status Ongoing
FDA Enforcement Report → search event 96005
Reason (FDA): The hermetic seal on the lid of the cans may be compromised
Where it went (FDA): Only in the US. States: AL, AR, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NH, NJ, NY, OH, OK, PA, SC, TN, TX, VA, WI
Recalling firm: Tipp Distributors, Inc. dba Novamex, El Paso, TX
FDA recall event 95750 · status Ongoing
FDA Enforcement Report → search event 95750
Reason (FDA): Patulin. Apple Cider was found to have elevated levels of patulin after receiving analytical testing results from 3rd party laboratory. Lab sample detected 78 ppb; limit is 50 ppb.
Where it went (FDA): Products were shipped to GA, NC, SC and FL.
Recalling firm: Apple Wedge LLC, Hendersonville, NC
FDA recall event 95496 · status Ongoing
FDA Enforcement Report → search event 95496
Reason (FDA): Required pasteurization temperatures were not achieved.
Where it went (FDA): US distribution to GA, NC, and SC.
Recalling firm: Big Bottom Milk Company, Rutherfordton, NC
FDA recall event 95276 · status Ongoing
FDA Enforcement Report → search event 95276
Reason (FDA): Foreign object - Soft plastic film
Where it went (FDA): Product was shipped to the following states: IA, IL, IN, KS, KY, MI, MN, MO, ND, NE, OH, SD & WI.
Recalling firm: KODIAK CAKES LLC, Park City, UT
FDA recall event 95236 · status Ongoing
FDA Enforcement Report → search event 95236
Reason (FDA): Elevated lead level 0.671 ppm in cacao (chocolate)
Where it went (FDA): Distributed to CA, FL, IL, KY, MD, ME, MI, MO, MT, NH, NY, OR, TX, UT, and WI.
Recalling firm: Inner Waymark LLC, Portland, OR
FDA recall event 95213 · status Ongoing
FDA Enforcement Report → search event 95213
Reason (FDA): Elevated lead levels in cinnamon
Where it went (FDA): Distributed to wholesaler in NY
Recalling firm: Gutierrez Distributors, LLC, Passaic, NJ
FDA recall event 95048 · status Ongoing
FDA Enforcement Report → search event 95048
Reason (FDA): Potential foreign material - plastic
Where it went (FDA): Recalled product was shipped to 7 retail stores and 3 distribution centers in the following states. IL, MI, TX,OH,NJ,FL, and AZ.
Recalling firm: Izzio Artisan Bakery, LLC, Louisville, CO
FDA recall event 95029 · status Ongoing
FDA Enforcement Report → search event 95029
Reason (FDA): Potential metal contamination
Where it went (FDA): Texas
Recalling firm: H-E-B San Antonio Retail Support Center (SARSC), San Antonio, TX
FDA recall event 94529 · status Ongoing
FDA Enforcement Report → search event 94529
Reason (FDA): Romaine lettuce may be contaminated with deer feces.
Where it went (FDA): IA, MN, ND, WI
Recalling firm: G.O. Corporation, Minneapolis, MN
FDA recall event 92828 · status Ongoing
FDA Enforcement Report → search event 92828
Reason (FDA): The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Where it went (FDA): Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
Recalling firm: TruVision Health LLC, Draper, UT
FDA recall event 92173 · status Ongoing
FDA Enforcement Report → search event 92173
Reason (FDA): Foreign Material - plastic
Where it went (FDA): IN
Recalling firm: Minn Dak Growers, Ltd., Grand Forks, ND
FDA recall event 90630 · status Ongoing
FDA Enforcement Report → search event 90630
Reason (FDA): The firm was notified by their rice supplier that the product may contain small pieces of glass.
Where it went (FDA): Product was shipped to the following states: GA, IL, KY, MA, MO, NJ, NY, RI, TX & UT.
Recalling firm: Kabobs Acquisition Inc., Lake City, GA
FDA recall event 90612 · status Ongoing
FDA Enforcement Report → search event 90612
Reason (FDA): Elevated levels of lead
Where it went (FDA): Distribution pattern is unknown. Product was sold to online customers and a customer list was not provided after multiple requests.
Recalling firm: A & E Corrales LLC, Seattle, WA
FDA recall event 89537 · status Ongoing
FDA Enforcement Report → search event 89537
Reason (FDA): The firm found small pieces of metal in the bakery palm oil silo which were not able to be detected every pass through the metal detector.
Where it went (FDA): Product was shipped to the following states: CA, NY, PA, WA.
Recalling firm: Poppies International INC, Battleboro, NC
FDA recall event 89319 · status Ongoing
FDA Enforcement Report → search event 89319
Reason (FDA): The firm was notified by the FDA that the product contains the unapproved food additive 1,4-dimethylamylamine (DMAA).
Where it went (FDA): The product was shipped to the following states: AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MO, MS, MT, NC, NE, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, VT, WA & WI.
Recalling firm: Hi Tech Pharmaceuticals, Norcross, GA
FDA recall event 87919 · status Ongoing
FDA Enforcement Report → search event 87919
Reason (FDA): The firm was notified via a customer complaint that they found foreign objects in the packaging of the product.
Where it went (FDA): Product was shipped to the following states: AL, AZ, CA, CO, CT, FL, GA, IL, KY, LA, MA, MD, MI, MN, MO, NC, NJ, OH, OR, PA, TX, UT, WA & WI. Product was also shipped to Canada.
Recalling firm: Genpak, Charlotte, NC
FDA recall event 87806 · status Ongoing
FDA Enforcement Report → search event 87806
Reason (FDA): The firm is recalling their products due the unapproved use of a food additive and unapproved marketing statements
Where it went (FDA): Product was shipped nationwide to all 50 states
Recalling firm: Fusion Health and Vitality LLC, Alpharetta, GA
FDA recall event 86773 · status Ongoing
FDA Enforcement Report → search event 86773
Reason (FDA): They were notified by their supplier that the product may be contaminated with foreign material.
Where it went (FDA): Product was shipped to the following states: AL, AZ, CA, CT, FL, GA, IL, IN, KS, MD, MI, NC, NJ, NY, OH, PA & TX.
Recalling firm: Sugar Foods Corporation, New York, NY
FDA recall event 84711 · status Ongoing
FDA Enforcement Report → search event 84711
Reason (FDA): The firm found what appeared to be plastic in the product.
Where it went (FDA): Product was shipped to the following states: GA, IN, LA, MN, MO, NC, OH, OK, TX & WY.
Recalling firm: Bake One, Inc., Smyrna, GA
FDA recall event 81195 · status Ongoing
FDA Enforcement Report → search event 81195
Reason (FDA): Product contains plastic material.
Where it went (FDA): Product was shipped to IL, IN, KY, MI, OH & WV.
Recalling firm: COCA COLA BOTTLING COMPAN, Charlotte, NC
FDA recall event 81016 · status Ongoing
FDA Enforcement Report → search event 81016
Reason (FDA): The firm was informed that the product did not contain vitamin B12 (Methylcobalamyn) as listed on the label.
Where it went (FDA): Product was shipped to the following states: AL, CA, FL, GA, IL, IN, KY, MD, MA, MO, MT, NV, NJ, NY, NC, OH, OK, PA, TN, TX, UT & VA.
Recalling firm: Absonutrix, Greensboro, NC
FDA recall event 80241 · status Ongoing
FDA Enforcement Report → search event 80241
Reason (FDA): Foreign material (rubber) detected in product.
Where it went (FDA): GA
Recalling firm: National Sugar Marketing LLC, Savannah, GA
FDA recall event 76470 · status Ongoing
FDA Enforcement Report → search event 76470
Reason (FDA): Possible contamination with foreign matter; wood pieces.
Where it went (FDA): CT, FL, GA, MA, MD, NC, NJ, NY, PA, SC, and VA.
Recalling firm: Inland Seafood, Inc., Tucker, GA
FDA recall event 75003 · status Ongoing
FDA Enforcement Report → search event 75003
Reason (FDA): Product contains elevated levels of lead.
Where it went (FDA): Distributed within the state of Florida and in the following countries: France, Jamaica, Columbia, Dominican Republic, Barbados, Honduras, St John Antigua
Recalling firm: Spices USA Inc., Hialeah, FL
FDA recall event 75282 · status Ongoing
FDA Enforcement Report → search event 75282
Reason (FDA): Inaccurate Nutrition Facts information listed on product
Where it went (FDA): The adulterated product was distributed to the following states: AZ,MD,NM,WI,CO,HI,MO, IA, GA, SC, WA,PA, IL, CA, OR, TX,FL, NH,LA,KS,MS, OK,MO,MN, MI, TN, NY, NV, UT, OH, NJ, AK,VA, AL, ME
Recalling firm: Unilever North America Supply Chain Company, LLC, Englewood Cliffs, NJ
FDA recall event 99757 · status Ongoing
FDA Enforcement Report → search event 99757
Reason (FDA): Product has the potential to be spoiled.
Where it went (FDA): Distributed throughout the United States.
Recalling firm: Horizon Organic Dairy, LLC, Broomfield, CO
FDA recall event 99605 · status Ongoing
FDA Enforcement Report → search event 99605
Reason (FDA): Undeclared FD&C Red No. 40
Where it went (FDA): NY, NJ, PA
Recalling firm: Wonton Specialists, Brooklyn, NY
FDA recall event 99508 · status Ongoing
FDA Enforcement Report → search event 99508
Reason (FDA): Inaccurately declared nutrients including Carbohydrates (understated) and Cholesterol (understated).
Where it went (FDA): AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI.
Recalling firm: Prospector Popcorn, LLC, Ridgefield, CT
FDA recall event 99434 · status Ongoing
FDA Enforcement Report → search event 99434
Reason (FDA): Potential for spoilage.
Where it went (FDA): Domestic: AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, MD, ME, MI, MO, NC, NH, NJ, NV, NY, OH, PA, SC, SD, TN, TX, VA, WA, WI. Foreign: Canada.
Recalling firm: AMY'S KITCHEN INC., Petaluma, CA
FDA recall event 99306 · status Ongoing
FDA Enforcement Report → search event 99306
Reason (FDA): Undeclared colors (FD&C Yellow 5 and FD&C Red 40).
Where it went (FDA): NY, NJ
Recalling firm: Alb-USA Enterprises Inc, Bronx, NY
FDA recall event 99198 · status Ongoing
FDA Enforcement Report → search event 99198
Reason (FDA): Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.
Where it went (FDA): Product is available nationwide and sold through the firm's online website direct to consumers.
Recalling firm: SENSORY SUPPLEMENT LLC, Beverly Hills, CA
FDA recall event 99116 · status Ongoing
FDA Enforcement Report → search event 99116
Reason (FDA): May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
Where it went (FDA): Distributed in the following states: NJ, CT, NY, PA.
Recalling firm: D'Dioses Fruit Pops, Inc., Paterson, NJ
FDA recall event 99040 · status Ongoing
FDA Enforcement Report → search event 99040
Reason (FDA): Contains undeclared FD&C Yellow 6
Where it went (FDA): CT, GA, IL, MA, MD, NJ, NY, OH, PA, TX, UT, VA
Recalling firm: Hadson (Toko) Trading Co. Inc., Maspeth, NY
FDA recall event 98780 · status Ongoing
FDA Enforcement Report → search event 98780
Reason (FDA): A sample of the product had the active ingredient in a quantity greater than the labeled specification.
Where it went (FDA): Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers
Recalling firm: Shaman Botanicals, LLC, North Kansas City, MO
FDA recall event 98420 · status Ongoing
FDA Enforcement Report → search event 98420
Reason (FDA): Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40
Where it went (FDA): NY, MA
Recalling firm: KPCM New York Inc., Maspeth, NY
FDA recall event 98363 · status Ongoing
FDA Enforcement Report → search event 98363
Reason (FDA): Potential adulteration with erucic acid from mustard oil ingredient.
Where it went (FDA): U.S. Distribution: CA, NV, OR, UT, WA. Foreign Distribution: None.
Recalling firm: Mangalm LLC, Newark, CA
FDA recall event 98389 · status Ongoing
FDA Enforcement Report → search event 98389
Reason (FDA): Product contains undeclared Yellow #5
Where it went (FDA): Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MI, MO, MS, NC, NE, NH, NJ, NY, OH, OK, OR, PA, TN, TX, UT, VA & WI.
Recalling firm: Palmetto Gourmet Foods Inc., Saluda, SC
FDA recall event 98313 · status Ongoing
FDA Enforcement Report → search event 98313
Reason (FDA): Contains undeclared allergen (wheat) and colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).
Where it went (FDA): NJ, NY
Recalling firm: Bader Enterprises, Inc., Brooklyn, NY
FDA recall event 98398 · status Ongoing
FDA Enforcement Report → search event 98398
Reason (FDA): Product contains salt and is mislabeled
Where it went (FDA): U.S. Distribution: CA, CO, IL, IN, MI, NC, NY, OH, OR, PA, TX, UT, WA
Recalling firm: Organic Spices, Inc, Fremont, CA
FDA recall event 98296 · status Ongoing
FDA Enforcement Report → search event 98296
Reason (FDA): Recall is due to a misprint on the label that incorrectly identifies the total caffeine content on the can. The item contains 300mg of caffeine, instead of 150mg as provided on the can.
Where it went (FDA): Nationwide
Recalling firm: Fazt & Loud LLC, Dallas, TX
FDA recall event 98093 · status Ongoing
FDA Enforcement Report → search event 98093
Reason (FDA): The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
Where it went (FDA): The adulterated product was distributed to the following states: AR, GA, IA, IN, KY, MD, MN, NE, NY, OH, PA, TN, TX, VA, WA.
Recalling firm: SB FOOD LLC, Silver Spring, MD
FDA recall event 98385 · status Ongoing
FDA Enforcement Report → search event 98385
Reason (FDA): Undeclared FD&C Red #40
Where it went (FDA): New York
Recalling firm: Kosher First LLC, Brooklyn, NY
FDA recall event 98005 · status Ongoing
FDA Enforcement Report → search event 98005
Reason (FDA): Undeclared Milk and FD&C Blue #1.
Where it went (FDA): U.S. Distribution: TN
Recalling firm: Dough-To-Go Inc, Santa Clara, CA
FDA recall event 97937 · status Ongoing
FDA Enforcement Report → search event 97937
Reason (FDA): Undeclared Almonds, Sesame, Red 40, Red 3, and Blue 1
Where it went (FDA): Firm notified FDA of recall initiated by state of CT on 09/10/25. A copy of CT press release was requested for posting by FDA. Firm notified customers on 09/11/25.
Recalling firm: Gina Marie Bakery LLC, Waterbury, CT
FDA recall event 97587 · status Ongoing
FDA Enforcement Report → search event 97587
Reason (FDA): Undeclared Yellow #5 and Yellow #6.
Where it went (FDA): U.S. consignees: AK, AZ, CA, CO, GA, IL, IN, LA, MA, MI, MN, MT, NC, NH, NJ, NM, NV, NY, OR, PA, SC, TX, UT, VA, WA, WY
Recalling firm: Itacate Foods LLC, Sacramento, CA
FDA recall event 97492 · status Ongoing
FDA Enforcement Report → search event 97492
Reason (FDA): Mislabeling
Where it went (FDA): FL
Recalling firm: Alpine Slicing and Cheese Conversion Company, Monroe, WI
FDA recall event 97189 · status Ongoing
FDA Enforcement Report → search event 97189
Reason (FDA): Undeclared colors (FD&C Yellow #5, FD&C Blue #1, and FD&C Red #40)
Where it went (FDA): NY, NJ
Recalling firm: Nature's Eudos Distributors LLC, Milford, CT
FDA recall event 96963 · status Ongoing
FDA Enforcement Report → search event 96963
Reason (FDA): Misbranded - label states 2g total carbohydrates instead of 27g
Where it went (FDA): MA, NC, IL, WI, TX, CA, MD, OK, FL
Recalling firm: Victor Packing Inc., Madera, CA
FDA recall event 96530 · status Ongoing
FDA Enforcement Report → search event 96530
Reason (FDA): Labeling Error. Nutren 2.0 UltraPak pouches were mislabeled with an Isosource 1.5 label.
Where it went (FDA): AZ, CA, FL, GA, IL, IN, LA, MA, MD, MO, MS, NY, OH, PA, TX, VA
Recalling firm: NESTLE HEALTH SCIENCE, Bridgewater, NJ
FDA recall event 95710 · status Ongoing
FDA Enforcement Report → search event 95710
Reason (FDA): The firm received complaints of a "rancid taste" from consumers.
Where it went (FDA): IL & PA
Recalling firm: Legally Addictive Foods, Weaverville, NC
FDA recall event 95663 · status Ongoing
FDA Enforcement Report → search event 95663
Reason (FDA): Mislabeled. Cans of regular Minute Made Lemonade were placed in cartons labeled Minute Maid Zero Sugar Lemonade.
Where it went (FDA): Product was shipped to retail stores located in the following states: IN, KY & OH.
Recalling firm: COCA COLA Consolidated LLC, Charlotte, NC
FDA recall event 95317 · status Ongoing
FDA Enforcement Report → search event 95317
Reason (FDA): During an inspection by NCDA, the firm was notified that the label does not list any ingredients in the product.
Where it went (FDA): Products were shipped to the following states: GA, NC & SC
Recalling firm: Robeson Enterprises, Mount Holly, NC
FDA recall event 94151 · status Ongoing
FDA Enforcement Report → search event 94151
Reason (FDA): During an internal investigation, the firm noticed that the Retort Chart was malfunctioning. No data was recorded during the production run.
Where it went (FDA): Product was shipped to Florida, Texas and Virginia.
Recalling firm: Moody Dunbar Inc, Johnson City, TN
FDA recall event 92838 · status Ongoing
FDA Enforcement Report → search event 92838
Reason (FDA): During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5.
Where it went (FDA): Product was shipped to the following states: AL, FL, GA, NC, SC & TN
Recalling firm: BAPS Shayona, Lilburn, GA
FDA recall event 92774 · status Ongoing
FDA Enforcement Report → search event 92774
Reason (FDA): Macarons do not declare the following colors: FD&C Blue #1, Blue #2, Red #3, Yellow #5, Yellow #6, Red #40.
Where it went (FDA): WI
Recalling firm: Elegant Foods, LLC, Madison, WI
FDA recall event 89890 · status Ongoing
FDA Enforcement Report → search event 89890
Reason (FDA): Product contains insufficient Higenamine and the label incorrectly declares Cayenne Pepper (CapsiMax) and Choline Bitartrate.
Where it went (FDA): Product was distributed to the following states: AL, FL, GA, NM, TN & TX.
Recalling firm: Nexagen, LLC, Fayetteville, GA
FDA recall event 82853 · status Ongoing
FDA Enforcement Report → search event 82853
Reason (FDA): Red 40 & Red 3 were not listed in the ingredients statement
Where it went (FDA): Product was shipped to the following states: AL, CA, GA, OH, OK & PA.
Recalling firm: Byrd Cookie Co, Savannah, GA
FDA recall event 80447 · status Ongoing
FDA Enforcement Report → search event 80447
Reason (FDA): Ingredient statement for Lyrical Foods Mushroom and Ricotta Flavor Ravioli does not include the ingredient of garlic.
Where it went (FDA): US only to distributors in MD, MA, CA, FL, IN, WA and TX
Recalling firm: Lyrical Foods Inc, Hayward, CA
FDA recall event 77263 · status Ongoing
FDA Enforcement Report → search event 77263
WASHINGTON, October 6, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for canned chicken Vienna-style sausages that were illegally imported from Jamaica, a country that is not eligible to export meat or poultry products to the United States. FSIS is continuing to investigate how these products entered the country.
The following products are subject to the public health alert, regardless of the product date [view labels]:
140-g. cans of “GRACE READY TO EAT CHICKEN VIENNA SAUSAGES.”
140-g. cans of “GRACE READY TO EAT CHICKEN VIENNA SAUSAGES HOT & SPICY.”
The products bear establishment number “EST. NO G-01” inside the Jamaica mark of inspection. The importer subsequently distributed the product to retail locations in Alabama, Florida, Georgia, Maryland, and Texas.
The problem was discovered during routine FSIS surveillance activities of imported products in commerce.
There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about an illness or injury should contact a health care provider.
FSIS is concerned that some product may be in consumers’ pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Sandra Campbell, owner, at 305‑887‑9523 or purecaribbeandist@gmail.com .
| Brand Name | Product Name | Size | Use By Dates | Stores Affected | States Affected |
|---|---|---|---|---|---|
| Deli Kitchen | Chipotle Cheddar Chicken Wrap | 9.25 oz | 8/07/2026 - 8/13/2026 | Kroger/Dillons | KS, MO, NE, TX, LA, OH, MI, IN, IL, KY, WV |
| Deli Kitchen | Cajun Chicken Mashed Potatoes & Corn | 11.5 oz | 8/07/2026 - 8/14/2026 | Kroger | TX, KS, NE, LA |
| H-E-B | Shake Rattle Bowl Southwest Chicken | 9.75 oz | 8/07/2026 - 8/15/2026 | H-E-B | TX |
| Higher Harvest for H-E-B | Chicken & Beef Chimichurri | 12 oz | 8/6/2026, 8/9/2026, 8/13/2026 | H-E-B | |
| Higher Harvest for H-E-B | Creamy Cilantro Chicken | 13 oz | 8/4/2026, 8/5/2026, 8/8/2026, 8/11/2026, 8/12/2026 | H-E-B | TX |
| Marketside | Marketside Southwest Style Salad with Chicken | 12.5 oz | 8/08/2026 - 8/16/2026 | Walmart | FL, LA, OK, TX, NE, MO |
| Meal Simple | Pork Carnitas Bowl | 11 oz | 8/3/2026, 8/7/2026, 8/10/2026, 8/14/2026 | H-E-B | TX |
| Meal Simple | Chicken & Rice with Cilantro Jalapeno Sauce | 12 oz | 8/3/2026, 8/7/2026, 8/10/2026, 8/14/2026 | H-E-B | TX |
| RaceTrac | Southwest Style Salad Chicken | 9.25 oz | 8/07/2026 - 8/13/2026 | RaceTrac | TX, AL |
| Ready Meals | Beef Barbacoa Bowl Premade | 12.5 oz | 8/07/2026 - 8/12/2026 | Albertsons, Randalls, Tom Thumb | AR, LA, OK, TX |
| Ready Meals | Chile Lime Rice Chicken Bowl Premade | 14.75 oz | 8/07/2026 - 8/12/2026 | Albertsons, Randalls, Tom Thumb | AR, LA, OK, TX |
| Ready Meals | Pork Chile Verde Bowl Premade | 14.1 oz | 8/07/2026 - 8/12/2026 | Albertsons, Randalls, Tom Thumb | AR, LA, OK, TX |
| Ready Meals | Chipotle Chicken Wrap | 9.5 oz | 8/08/2026 - 8/11/2026 | Albertsons, Randalls, Tom Thumb | AR, LA, OK, TX |
| Taylor Farms | Classic Beef Burrito | 12.8 oz | 8/07/2026 - 8/12/2026 | Hannaford | ME, NH, MA, NY, VT |
| Taylor Farms | Chipotle Chicken Tortilla Wrap | 10.3 oz | 8/07/2026 - 8/10/2026 | Hannaford | NY, CT, NJ, ME, NH, VT, MA, RI |
| Taylor Farms | Chicken Verde Burrito | 12 oz | 8/07/2026 - 8/10/2026 | Hannaford | ME, NH, MA, NY, VT |
| Taylor Farms | Chicken Enchilada | 4/34.5 oz | 8/07/2026 - 8/16/2026 | Kroger | KS, LA, NE, TX |
| Wawa | Spicy Chipotle Chicken Wrap | 6.9 oz | 8/06/2026 - 8/08/2026 | Wawa | TN, OH, IN, KY |
Source: official product list (PDF)
WASHINGTON, Aug. 8, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for meat and poultry products containing FDA-regulated jalapeños that may be contaminated with Salmonella. FSIS expects additional downstream products will be identified as this ingredient recall progresses. As more information becomes available, FSIS will update this public health alert. Consumers should check back frequently.
The list of products subject to the public health alert is available here, including information such as the product names, establishment numbers, states where the products were distributed, and contact information for media and consumers.
The problem was discovered when FDA notified FSIS that multiple FSIS-regulated establishments received an FDA-regulated ingredient that had been recalled. More information on the FDA recall and outbreak investigation is available on FDA’s website.
Consumption of food contaminated with Salmonella can cause salmonellosis, one of the most common bacterial foodborne illnesses. The most common symptoms of salmonellosis are diarrhea, abdominal cramps, and fever within 6 hours to 6 days after eating the contaminated product. The illness usually lasts 4 to 7 days. Most people recover without treatment. In some persons, however, the diarrhea may be so severe that the patient needs to be hospitalized. Older adults, infants, and persons with weakened immune systems are more likely to develop severe illness. Individuals concerned about an illness should contact their health care provider.
There have been no confirmed reports of illness due to consumption of the FSIS-regulated products containing the affected jalapeños. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ or retailers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. Retailers who have purchased these products are urged not to serve or sell them. These products should be thrown away or returned to the place of purchase.
WASHINGTON, JUL 30, 2026 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for Curry Chicken Salad due to concerns that the product may be contaminated with Listeria monocytogenes (Lm). A recall was not requested because the products are no longer available for purchase.The Curry Chicken Salad item was produced on July 22, 2026. The following product subject to the public health alert is [view labels]:8-oz. plastic packages containing portions of "CURRY CHICKEN SALAD" with a USE BY: 07/30/2026 printed on the back label.The products bear establishment number "P-39928" inside the USDA mark of inspection. These items were shipped to retail locations in Oregon and Washington.The problem was discovered during routine establishment testing.There have been no confirmed reports of illness due to consumption of these products. Anyone concerned about an illness should contact a health care provider.Consumption of food contaminated with Lm can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.FSIS is concerned that some product may be in consumers' refrigerators. Consumers who have purchased these products are urged not to consume them.These products should be thrown away or returned to the place of purchase.Media and consumers with questions regarding the public health alert can contact Ernie Spada Jr., Sr. Vice President/Owner of Mary's Harvest Fresh Foods, Inc., at (503)-288‑8300 or eiii@mlffv.com.
WASHINGTON, Jul 29, 2026 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for a Steak, Cilantro, Lime Burrito product due to misbranding and an undeclared allergen. The product contains egg, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to egg products are aware that this product should not be consumed. A recall was not requested because the affected product is no longer available for purchase.The Steak, Cilantro, Lime Burrito product was produced on Jun 19, 2026. The following product is subject to the public health alert [view labels]:3-lb 2-oz. carton containing 10 individually wrapped "RED'S STEAK CILANTRO AND LIME BURRITO" on the front package label with production lots, L1 SD6170 1503, L1 SD6170 1535, L1 SD6170 1606, L1 SD6170 1639, L1 SD6170 1717, L1 SD6170 1750, L1 SD6170 1831, L1 SD6170 1908, L1 SD6170 1954, L1 SD6170 2031, L1 SD6170 2108, L1 SD6170 2130 on the side of the package label.The individual products bear the establishment number "EST. 46069" inside the USDA mark of inspection. These items were shipped to Costco distribution locations in Illinois, Michigan and Minnesota.The problem was discovered by a consumer that identified the product contained in the carton of "RED'S STEAK CILANTRO AND LIME BURRITO" was a different product, which contains egg, and had been incorrectly labeled. The consumer reported the issue to the producing establishment, and the establishment notified FSIS.There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.FSIS is concerned that some product may be in consumers' freezers. Consumers who have purchased this product are urged not to consume it. The product should be thrown away or returned to the place of purchase.Media and consumers with questions regarding the public health alert can contact Andrea Breen, Chief Supply Chain Officer, Red's All Natural, at 203‑437‑7713, or andrea.breen@redsallnatural.com.
WASHINGTON, JULY 3, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for a beef jerky product due to misbranding and undeclared allergen. The product contains wheat, a known allergen, which is not declared on the product label. A recall was not requested because the product is no longer available for purchase.
The ready-to-eat beef jerky item was produced on various dates between August 7, 2025, and July 1, 2026. The following product is subject to the public health alert [view labels]:
2.5-oz. plastic bag packages of “STREET’S BEEF Jerky TERIYAKI FLAVOR” with lot codes 0701271, 0520271, 04014271, 0415271, 0211271, 1015261, 1016261, 1029261, 0909261, 0806261, and 0820261 shown on a sticker on the packaging.
The product bears establishment number “EST. 21827” inside the USDA mark of inspection. This item was shipped to three retail locations in Oklahoma: Bordwine Hay, Feed & Hardware, Grassroots Farm Store, and Bromide Trading Co.
The problem was discovered during a routine FSIS label review.
There have been no confirmed reports of adverse reactions due to consumption of this product. Anyone concerned about a reaction should contact a health care provider.
FSIS is concerned that some product may be in consumers’ pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Allyson Moore, Owner/Operator of GoodTimes Beef Jerky, at 405‑550‑7657 or goodtimesjerky@gmail.com.
WASHINGTON, JUNE 25, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for raw boneless chicken breast products due to misbranding and undeclared allergens. The product contains eggs, a known allergen, which is not declared on the product label. A recall was not requested because the product is no longer available for purchase.
The raw honey Dijon boneless chicken breast products were produced on June 2, 2026. The following product subject to the public health alert is [view labels]:
21-oz. vacuum-packed packages of “PRIVATE SELECTION Honey Dijon Boneless Skinless Chicken Breasts with Rib Meat” with “BEST IF USED BY: JUN 28 2026” and lot code “15326A” printed on the packaging.
The products bear establishment number “P-45288B” printed on the packaging. These items were shipped to Kroger and Fred Meyer retail stores in Alabama, Alaska, Idaho, Illinois, Indiana, Kentucky, Tennessee, Oregon, and Washington.
The problem was discovered by a retailer after a store employee identified that the correct label was applied to the front of the product but the incorrect label, which contained the ingredients statement, was applied to the back of the product. The retailer reported the issue to the producing establishment, and the establishment notified FSIS.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a health care provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers with questions regarding the public health alert can contact FW Farms LLC Customer Service at cs@gwfg.com. Members of the media with questions regarding the public health alert can contact FW Farms LLC at media@gwfg.com.
WASHINGTON, June 25, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat chicken Caesar wrap products due to concerns that the product may be contaminated with Listeria monocytogenes (Lm). A recall was not requested because the products are no longer available for purchase.
The ready-to-eat chicken Caesar wrap items were produced on June 16, 2026. The following products subject to the public health alert are [view labels]:
8.7-oz. clear plastic wrapped packages of “FRESH SEASONS Kitchen Chicken Caesar Wrap” with “Sell By:6/24/2026” printed on the back label above the ingredients.
The products bear establishment number “P- 45091” inside the USDA mark of inspection. These products were shipped to Holiday convenience stores in Minnesota and Wisconsin.
The problem was discovered during routine FSIS product testing when a sample confirmed positive for the presence of Listeria monocytogenes.
There have been no confirmed reports of illness due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumption of food contaminated with Lm can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Jill Teut, Communications, Taher Inc., at communications@taher.com.
Editor's Note - June 1, 2026: Whole genome sequencing results show that the beef kofta samples collected by FSIS and produced at Olympia Food Industries (Est. 18743) matched the outbreak strain of E. coli O157:H7. FSIS continues to coordinate with the California Department of Public Health and local health departments in California on the outbreak investigation.
WASHINGTON, May 24, 2026 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that beef kofta products served at The Kebab Shop restaurant locations may be contaminated with Shiga toxin-producing E. coli (STEC) O157:H7. A recall was not requested because the products are no longer available for purchase.
The beef kofta was produced as a raw ground beef product by Olympia Food Industries, Inc. dba Olympia Foods (Est. 18743) in Franklin Park, Illinois, on January 6, 2026, and supplied to The Kebab Shop restaurant locations in California, Texas, and Florida.The problem was discovered as part of an ongoing illness outbreak investigation. FSIS, the California Department of Public Health (CDPH), and local health departments in California are investigating a localized outbreak of E. coli O157:H7 that includes 9 sick people in California. As of May 24, 2026, illness onset dates have been reported ranging from March 27, 2026, to April 30, 2026. Because the identified illnesses are limited to California, CDPH is leading this investigation with FSIS. FSIS continues to keep its federal partners informed as the investigation progresses. FSIS collected raw ground beef kofta product samples that tested positive for E. coli O157:H7. Further testing is ongoing to determine if the product samples are related to the specific outbreak strain.
FSIS is issuing this public health alert to ensure that consumers in California, Texas, and Florida are aware of the outbreak. The Kebab Shop stopped selling beef kofta at all of its restaurant locations on May 18, 2026.
E. coli O157:H7 is a potentially deadly bacterium that can cause dehydration, bloody diarrhea and abdominal cramps 2 to 8 days (3 to 4 days, on average) after exposure to the organism. While most people recover within a week, some develop a type of kidney failure called hemolytic uremic syndrome (HUS). This condition can occur among persons of any age but is most common in children under 5 years old and older adults. It is marked by easy bruising, pallor, and decreased urine output. Consumers who ate beef kofta from any location of The Kebab Shop and develop symptoms of STEC infection within 10 days of exposure should contact their health care provider. Consumers should discard any leftover beef kofta from The Kebab Shop.
As a general food safety practice, FSIS advises consumers to cook all ground beef products to an internal temperature of 160 degrees F, verified with a food thermometer. More information is available at https://www.fsis.usda.gov/safetempchart.
Media and consumers with questions regarding the public health alert can contact The Kebab Shop at 888‑965‑5821 or FoodSafety@thekebabshop.com.
Editor’s Note – May 14, 2026: Whole genome sequencing results show that headcheese samples collected by FSIS and produced at Crawford Sausage Co. (Est. 21406) tested positive for the outbreak strain of Listeria monocytogenes. FSIS continues to coordinate with the Illinois public health and agriculture partners on the outbreak investigation.
WASHINGTON, May 9, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for headcheese that may be contaminated with Listeria monocytogenes (Lm). A recall was not requested because the products are no longer available for purchase. Headcheese is a ready-to-eat (RTE), pork deli meat product typically made from meat and seasonings that are cooked together and formed into a loaf or jelly-style product.
The fully cooked pork headcheese products were produced on January 20, 2026. These products are intended for slicing at retail delis and some deli purchases may only show the producer’s brand without the affected date. The following products are subject to the public health alert [view labels]:
Various weight packages packed or sliced in retail delis, containing “DAISY BRAND Meat Products HEADCHEESE,” with a “USE BY” date of “MAR 26 2026.”
Various weight packages packed or sliced in retail delis, containing “DAISY BRAND Meat Products HEADCHEESE,” with a red sticker indicating “HOT” and a “USE BY” date of “MAR 26 2026.”
The products bear establishment number “EST. 21406” inside the USDA mark of inspection. These items were distributed to retail deli locations in Illinois and Indiana.
The problem was discovered as part of an ongoing illness outbreak investigation. FSIS, the Illinois Department of Public Health, and local health departments in Illinois are investigating a localized outbreak of Lm that includes three sick people in Illinois. Because the outbreak is contained within the state, Illinois is leading this investigation with FSIS. FSIS continues to keep its federal partners at the Centers for Disease Control and Prevention informed as the investigation progresses. FSIS collected an unopened headcheese product sample that tested positive for Lm. Further testing is ongoing to determine if the product samples are related to the specific outbreak strain.
FSIS is concerned that recently purchased product may remain in consumer refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. Consumers who have purchased these products are also urged to clean refrigerators thoroughly to prevent the risk of cross-contamination.
Consumption of food contaminated with Lm can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS recommends retail delis clean and sanitize all food and non-food surfaces and discard any open meats and cheeses in the deli that housed the products subject to this alert. Retailers may refer to FSIS’ guideline, Best Practices Guidance for Controlling Listeria monocytogenes in Retail Delicatessens, for information on steps to prevent Lm contamination in RTE foods that are prepared or sliced in retail delis and consumed in the home, such as deli meats and deli salads.
Media and consumers with questions regarding the public health alert can contact the Crawford Sausage Co., Inc. at (773) 277 3095.
WASHINGTON, May 4, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ravioli pasta products due to misbranding and undeclared allergens. The ravioli labeled as beef and burrata may actually contain shrimp filling in lobster sauce. The shrimp and lobster, known allergens (shellfish), are not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with shellfish allergies are aware that this product should not be consumed. A recall was not requested because the product is no longer available for purchase.
The ravioli pasta items were produced between March 10, 2026, and April 21, 2026. The following product is subject to the public health alert [view labels]:
32-oz. plastic bag packages containing “Giovanni Rana RANA Rustic Beef Sauce & Creamy Burrata Cheese Ravioli” with “use by” dates ranging 05/14/2026 – 06/25/2026.
The product bears establishment number “Est. 44870” inside the USDA mark of inspection. These items were shipped to Costco retail stores in Maryland and New Jersey.
The problem was discovered when the establishment notified FSIS that they received two consumer complaints reporting the beef sauce and burrata ravioli actually contained shrimp ravioli.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a health care provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact April Klein, Customer Service Manager, Rana Meal Solutions, at aklein@ranausa.us.
WASHINGTON, APRIL 30, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for meat and poultry products containing FDA-regulated dairy ingredients that may be contaminated with Salmonella. FSIS expects additional downstream products will be identified as this ingredient recall progresses. As more information becomes available, FSIS will update this public health alert. Consumers should check back frequently.
The list of products subject to the public health alert are available here, including information such as the establishment numbers and states where the products were distributed. The labels are available here.
The problem was discovered when FDA notified FSIS that multiple FSIS-regulated establishments received FDA-regulated ingredients formulated with dry milk powder that had been recalled.
Consumption of food contaminated with Salmonella can cause salmonellosis, one of the most common bacterial foodborne illnesses. The most common symptoms of salmonellosis are diarrhea, abdominal cramps, and fever within 6 hours to 6 days after eating the contaminated product. The illness usually lasts 4 to 7 days. Most people recover without treatment. In some persons, however, the diarrhea may be so severe that the patient needs to be hospitalized. Older adults, infants, and persons with weakened immune systems are more likely to develop severe illness. Individuals concerned about an illness should contact their health care provider.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a health care provider.
FSIS is concerned that some product may be in consumers’ or retailers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. Retailers who have purchased these products are urged not to serve or sell them. These products should be thrown away or returned to the place of purchase.
WASHINGTON, April 9, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for raw beef and pork products due to misbranding and an undeclared allergen. The products may contain sesame, a known allergen, which is not declared on the product label. A recall was not requested because the products are no longer available for purchase.
The raw beef and pork items were produced from December 1, 2025, through April 6, 2026. The following products are subject to the public health alert [view labels]:
1.5-lb. clear plastic containers with safety lids containing “QUALITY MEAT SKY RANCH PREMIUM PROVISIONS MARINATED BEEF RIBEYE ROLL /BULGOGI” with “SELL BY” dates of “DEC.11.25” through “APR.16.26”.
1.5-lb. clear plastic containers with safety lids containing “QUALITY MEAT SKY RANCH PREMIUM PROVISIONS MARINATED PORK TENDERIZED CT BUTT” with “SELL BY” dates of “DEC.11.25” through “APR.16.26”.
1.5-lb. clear plastic containers with safety lids containing “QUALITY MEAT SKY RANCH PREMIUM PROVISIONS MARINATED BEEF SLICED SHORT RIBS /LA STYLE” with “SELL BY” dates of “DEC.11.25” through “APR.16.26”.
1.5-lb. clear plastic containers with safety lids containing “QUALITY MEAT SKY RANCH PREMIUM PROVISIONS MRN PORK SINGLE BELLY CHOP / JUMULLEOK” with “SELL BY” dates of “DEC.11.25” through “APR.16.26”.
The products bear establishment number “EST. 1377” inside the USDA mark of inspection. These items were shipped to Lotte Plaza Market retail locations in Florida, Maryland, New Jersey, and Virginia.
The problem was discovered by FSIS personnel during a routine label review. FSIS personnel noticed the use of sesame oil in the products, but sesame was not declared as an ingredient on the label.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a health care provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Sang Min Lee, President, Sky Ranch Meat LLC, at 410‑290‑3643 ext. 9902 or a.lee@lotteplaza.com.
WASHINGTON, April 6, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is retracting the public health alert issued on April 1, 2026, for Walmart Great Value Fully Cooked Dino Shaped Chicken Breast Nuggets with “Best If Used By” date “Feb 10 2027” produced by Dorada Foods after confirming that the product does not pose a public health concern.
The public health alert was originally issued based on routine surveillance sampling conducted by the New York State Department of Public Health that indicated elevated trace levels of lead. Because this product is commonly consumed by children, FSIS issued the alert to inform consumers of a potential risk.
Following the alert, additional sampling was conducted by the New York State Department of Public Health and the producing establishment, Dorada Foods. As part of that process, the original lot of product was tested as well as additional lots.
All follow‑up testing, including testing of the original lot, found no elevated levels of lead in the product.
FSIS subsequently reviewed the underlying laboratory data in coordination with the New York State Department of Health and determined that the initial result was a false positive, caused by sporadic lead contamination at the laboratory during analysis, not contamination of the product itself. Follow up testing confirmed no elevated levels of lead were present in any of the products tested.
FSIS has therefore concluded that the product does not pose a public health concern.
FSIS has notified the company and is updating this page to ensure consumers have accurate and up-to-date information.
Product Images
PHA-04012026‑01.pdf
Company Information
Dorada Foods
Ponca City, OK
Establishment ID
M44164+P44164
Company Contact Information
Company Contact
Dorada Foods
John Patrick Lopez
john.patrick@lopezdorada.com
Processing Category
Fully Cooked - Not Shelf Stable
FSIS Contact Information
Media Contact
Congressional and Public Affairs
Bailey McWilliams
FSISpress@usda.gov
Last Updated: Apr 06, 2026
Editor’s Note: Mar. 30, 2026 – The labels in this release were revised to remove unrelated product that was inadvertently included in the background of some photos.
WASHINGTON, March 25, 2026 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for various raw beef and pork products that were produced without the benefit of federal inspection and may bear a false mark of inspection. Food produced without inspection may contain undeclared allergens, harmful bacteria, or other contaminants that put consumer health and safety at risk. FSIS is continuing to investigate and may add additional products to this alert as more information is obtained.
The beef and pork items were produced from April 2024 through March 2026. The following products subject to the public health alert are [view labels]:
5-lb. box of 8-oz. packages containing a VACUUM-PACKED piece of "BLACKWING ORGANIC MEATS ORGANIC BEEF NEW YORK STRIP STEAK," with "EST. 1996" inside the USDA mark of inspection.
10-lb. box of 16-oz. packages containing a VACUUM-PACKED package of "BLACKWING ORGANIC MEATS ORGANIC GROUND BEEF."
5-lb. box of 8-oz. packages containing a VACUUM-PACKED package of "BLACKWING ORGANIC MEATS GRASS FED ORGANIC BEEF STEW MEAT," with "EST. 1996" inside the USDA mark of inspection.
5-lb. box of 8-oz. packages containing a VACUUM-PACKED piece of "BLACKWING ORGANIC MEATS ORGANIC BEEF STEAK STRIPS," with "EST. 1996" inside the USDA mark of inspection.
1-lb. VACUUM-PACKED package of "BLACKWING MEATS BLACKWING BEEF GROUND FROM ORGANIC BEEF," without USDA mark of inspection.
12-oz. VACUUM-PACKED package of "BLACKWING MEATS PORK GROUND MADE FROM ORGANIC PORK," without USDA mark of inspection.
12-oz. VACUUM-PACKED package of "BLACKWING MEATS Boneless Center Cut Pork Chops 2‑6oz Made from Organic Pork," without the USDA mark of inspection.
The first four products include the unauthorized use of establishment number "EST. 1996" inside a false USDA mark of inspection. These items were shipped to wholesale and retail locations nationwide.
The problem was discovered as part of an ongoing FSIS investigation.
There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about an illness or injury should contact a health care provider.
FSIS is concerned that some product may be in retailer or consumer freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Roger Gerber, Blackwing Meats, President, at 847‑838‑4888 or roger@blackwing.com.
WASHINGTON, March 23, 2026 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for a ground beef product that may be contaminated with foreign material, specifically metal. A recall was not requested because the product is no longer available for purchase.
The ground beef item was produced on Feb 26, 2026. The following product is subject to the public health alert [view labels]:
16oz (1 lb.) PLASTIC, VACUUM-PACKED, packages containing "WHITE OAK PASTURES, RADICALLY TRADITIONAL FARMING, GRASSFED GROUND BEEF".
The product bears establishment number "EST 34729" inside the USDA mark of inspection and is stamped on the back with "105761 Sell by 03/19/26". This item was shipped to a distributor, and Mom's Organic Markets retail locations in D.C., Mass., Md., N.J., Pa. and Va.
The problem was discovered by the establishment after receiving two complaints from consumers.
There have been no confirmed reports of injury due to consumption of this product. Anyone concerned about an injury should contact a health care provider. FSIS has received no additional reports of injury from consumption of these products.
FSIS is concerned that some product may be in consumers' freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Mr. Justin Wiley, Processing Operations Manager, White Oak Pastures, at (229) 641‑2081 or feedback@whiteoakpastures.com.
WASHINGTON, March 13, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for frozen ready-to-eat turkey stuffed pastry products due to misbranding. Some boxes of the turkey, pesto, and cheese stuffed pastries contain ham and cheese instead. A recall was not requested because the product is no longer available for purchase.
The turkey, pesto, and cheese stuffed pastries were packaged on Feb. 18, 2026, and may contain ham and cheese stuffed pastry items. The following product is subject to the public health alert [view labels]:
25.4-oz. boxes containing eight pieces of “LA BOULANGERIE TURKEY PESTO & SWISS CHEESE POCKETS” with lot code 04926 and “best by” date 02/18/27 printed on the packaging.
The products bear establishment number “P-51243A” inside the USDA mark of inspection. These items were shipped to Costco locations across the Midwest.
The problem was discovered when the establishment notified FSIS that it received two consumer complaints regarding turkey and cheese stuffed pastry boxes containing ham and cheese instead.
There have been no reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a health care provider.
FSIS is concerned that some mislabeled product may be in consumers’ freezers. Consumers who purchased this product should check their packaging to see if they have the affected item. The product may be returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Shaw Bakers LLC, at Complaints@shawbakers.com
WASHINGTON, March 1, 2026 – The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for beef jerky products due to misbranding and undeclared allergens. The products may contain soy lecithin, a known allergen, which is not declared on the product label. A recall was not requested because the products are no longer available for purchase.
The ready-to-eat beef jerky items bear best by dates of February 17, 2027 or prior. The following products subject to the public health alert are [view labels]:
6-oz. plastic packages containing "DRIED HAWAIIAN STYLE BEEF CRISPS, ORIGINAL SALT & PEPPER FLAVOR", and bearing establishment number "EST. 2625" inside the USDA mark of inspection.
4-oz. plastic packages containing "PUNAHELE JERKY COMPANY INC UNCLE K'S BEEF CRISPS".
4-oz. plastic packages containing "PUNAHELE JERKY COMPANY INC KILAUEA FIRE SPICY BEEF CRISPS".
These items were distributed to retail stores in Hawaii and sold via online sales nationwide.
The problem was discovered during a routine FSIS label review.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a health care provider.
FSIS is concerned that some product may be in consumers' pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Sabrina Vaughn, Food Safety and QA Compliance Officer, at 808‑961‑0877.
WASHINGTON, Oct. 7, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for FSIS-inspected ready-to-eat meals produced by FreshRealm containing a Food and Drug Administration (FDA) regulated ingredient, specifically riced cauliflower, that may be contaminated with Listeria monocytogenes (Lm). Based on current evidence, the products included in this public health alert are not related to any ongoing outbreak investigations. A recall was not requested because the products are no longer available for purchase.
The following products are subject to the public health alert [view labels]:
Sold by Blue Apron: 13.05-oz. plastic tray packages labeled "DISH by Blue Apron Cheesy Chicken Mac with Vegetables" with lot codes 25240 and 25247. The product bears establishment number "P-3081."
Sold by Marley Spoon: 10.5-oz. packages labeled “BALANCE by Marley Spoon BBQ Sauce Beef Meatballs with Cheesy Cauliflower” with lot code 25255. The product bears establishment number “Est. 47718.”
The problem was discovered when FreshRealm notified FSIS that the riced cauliflower used in these products tested positive for Listeria monocytogenes.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS is concerned that these products may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact FreshRealm’s customer service hotline at 1‑888‑244‑1562 or customerservice@freshrealm.com.
Editor’s Note: Details of this public health alert were updated on October 9, 2025, to reflect additional lot codes of the affected products.
Editor’s Note: Details of this public health alert were updated on October 7, 2025, to include information about the supplier’s recall of affected spinach and to indicate that the public health alert is not related to any ongoing outbreak investigations.
WASHINGTON, Oct. 6, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for FSIS-inspected ready-to-eat meals produced by FreshRealm containing a Food and Drug Administration (FDA) regulated ingredient, specifically spinach, that has been recalled by Sno Pac Foods due to possible contamination with Listeria monocytogenes (Lm). Based on current evidence, the products included in this public health alert are not related to any ongoing outbreak investigations.
FSIS expects additional affected products to be identified and will update this public health alert as more information becomes available. Consumers should check back frequently.
The following products are subject to the public health alert [view labels]:
10.1-oz. containers of “HELLO FRESH READY MADE MEALS CHEESY PULLED PORK PEPPER PASTA” with establishment number “Est. 47718” and lot code 49107 or establishment number “Est. 2937” and lot codes 48158 or 48840. This item was shipped directly to consumers by HelloFresh.
10-oz. containers of “HELLO FRESH READY MADE MEALS UNSTUFFED PEPPERS WITH GROUND TURKEY” with establishment number “P-47718” and lot codes 49569, 50069, 50073, or 50698. This item was shipped directly to consumers by HelloFresh.
The problem was discovered when FreshRealm notified FSIS that the spinach used in these products tested positive for Listeria monocytogenes.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS is concerned that these products may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact FreshRealm’s customer service hotline at 1‑888‑244‑1562 or customerservice@freshrealm.com.
Editor's Note: Details of this public health alert were updated on September 30, 2025, to account for additional Trader Joe's Cajun style chicken fettucine alfredo products that use the pasta that has been recalled due to possible Listeria contamination. Products with use by dates up until October 10, 2025, may be impacted. Please see details below and check back frequently to see if additional products have been added.
Editor's Note: Details of this public health alert were updated on September 29, 2025. FSIS and its public health partners, including the Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA), are investigating an outbreak of Listeria monocytogenes. Whole genome sequencing confirmed a sample of the pasta ingredient used in these meals is genetically related to the Listeria Outbreak Linked to Prepared Meals. For more details, view the CDC alert and the FDA advisory Outbreak Investigation of Listeria monocytogenes: Prepared Pasta Meals. FSIS will continue to update this alert if it identifies additional FSIS-regulated products that may be affected.
Editor's Note: Details of this public health alert were updated on September 26, 2025, to reflect an additional affected product and corresponding labels.
WASHINGTON, September 25, 2025 – The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat meals containing a Food and Drug Administration (FDA) regulated pre-cooked pasta that may be contaminated with Listeria monocytogenes (Lm). FSIS expects more updates as this investigation continues. As more information becomes available, FSIS will update this public health alert. Consumers should check back frequently
The following product are subject to the public health alert:
Sold at Walmart: 12-oz. clear plastic tray packages labeled "MARKETSIDE LINGUINE WITH BEEF MEATBALLS & MARINARA SAUCE" with "best if used by" dates SEP 22, 2025; SEP 24, 2025; SEP 25, 2025; SEP 29, 2025; SEP 30, 2025; and OCT 01, 2025. The product bears establishment number "EST. 50784" or "EST. 47718" inside the USDA mark of inspection. [view labels]
Sold at Trader Joe's: 16-oz. plastic tray packages labeled "TRADER JOE'S CAJUN STYLE BLACKENED CHICKEN BREAST FETTUCINE ALFREDO" with "best if used by" dates 9/20/2025, 9/24/2025, 9/27/2025, 9/28/2025, 10/01/2025, 10/03/2025, 10/05/2025, 10/08/2025, or 10/10/2025 printed on the front label of the packaging. The product bears establishment number "P- 45288" inside the USDA mark of inspection. [view labels]
One of the producing companies collected samples of the FDA-regulated, pre-cooked pasta used as an ingredient in its product as part of the ongoing investigation related to the Listeria outbreak linked to chicken fettuccine alfredo meals. The test confirmed that the linguine pasta was positive for Lm and further testing confirmed the Lm is genetically related to the specific outbreak strain. FSIS previously issued a recall notice linked to the Listeria outbreak in June and continues to coordinate with FDA, the Centers for Disease Control and Prevention, and state public health partners.
Consumption of food contaminated with Lm can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS is concerned that some product may be in consumers' refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers with questions regarding the public health alert can contact Nate's Fine Foods at 916‑677‑7303. Operating hours are between 9:00 a.m. and 4:00 p.m. PST Monday through Friday.
WASHINGTON, September 19, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for a ready-to-eat (RTE) turkey wrap product due to concerns that the product may be contaminated with Listeria monocytogenes. A recall was not requested because the affected product is no longer available for purchase.
The RTE turkey wrap product was produced on September 10, 2025. The following product is subject to the public health alert [view sample labels]:
10-oz. clear plastic clamshell packages containing “TRADER JOE’S TURKEY GOBBLER WRAP” with “BEST BY SEP 16, 2025.”
The product bears establishment number “P-1644” inside the USDA mark of inspection. This item was shipped to Trader Joe’s retail locations nationwide.
The problem was discovered when the establishment notified FSIS that food contact surface samples associated with this product tested positive for Listeria monocytogenes.
There have been no confirmed reports of adverse reactions due to consumption of this product. Anyone concerned about an illness should contact a health care provider.
Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased this product are urged not to consume it. The product should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Trader Joe’s Customer Relations at 626‑599‑3817, on Monday through Friday from 6:00 am to 6:00 pm Pacific Time.
WASHINGTON, Sept. 10, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for raw sirloin beef tip product due to misbranding and undeclared allergens. The product contains sesame and wheat, known allergens, which are not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to sesame and wheat are aware that these products should not be consumed. A recall was not requested because the affected products are no longer available for purchase.
The raw sirloin beef tip product was produced on September 2, 2025. The following product is subject to the public health alert [view labels]:
1-lb. vacuum-packed packages containing “Bianco & Sons SWEET HEAT SIRLOIN BEEF TIPS” on the front package label with “USE OR FREEZE BY:10/01/2025” on the back package label.
The products bear the establishment number “EST. 4033” inside the USDA mark of inspection. These items were shipped to Roche Bros. Supermarkets retail locations in Massachusetts.
The problem was discovered by a retailer that identified “Sweet Heat Sirloin Beef Tips” bearing the correct front label but incorrect back label for “Garlic and Ginger Sirloin Beef Tips.” The retailer reported the issue to the producing establishment, and the establishment notified FSIS.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some products may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Lewis Bianco, Chief Executive Officer, Bianco & Sons, at 781‑606‑1891 or lewis@biancosausage.com.
WASHINGTON, Aug. 29, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for a frozen not-ready-to-eat (NRTE) uncured pepperoni pizza product imported from Italy that did not receive the benefit of import reinspection. A recall was not requested because the product is no longer available for purchase.
The following product is subject to the public health alert [view labels]:
17.63-oz. cardboard box packages containing “TRADER JOE’S UNCURED PEPPERONI PIZZA PRODUCT OF ITALY” with “MFG LOT: 06/16/25 BEST BY: 08/16/26” or “MFG LOT: 06/21/25 BEST BY 08/21/26” printed on the bottom of the package.
The product bears the Italy establishment number “IT 1558 L UE” printed inside the Italian mark of inspection located on the front of the package. This item was shipped to retail locations in California.
The problem was discovered when FSIS was notified by Trader Joe’s Company that the frozen NRTE uncured pepperoni pizza product was not presented for FSIS import reinspection.
There have been no confirmed reports of illness or adverse reactions due to consumption of these products. Anyone concerned about an illness or reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased this product are urged not to consume it. This product should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Trader Joe’s Customer Relations at 626‑599‑3817.
WASHINGTON, July 30, 2025 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for frozen product labeled as pork and beef tortellini due to misbranding and undeclared allergens. The frozen product labeled as pork and beef tortellini may actually contain pork and beef toasted ravioli, which contains soy and sesame, known allergens, which are not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to soy and sesame are aware that this product should not be consumed. A recall was not requested because the products are no longer available for purchase.
The frozen product labeled as pork and beef tortellini that may contain pork and beef toasted ravioli was produced on May 27, 2025. The following product is subject to the public health alert [view labels]:
16-oz. bag "Schnucks Tortellini PORK & BEEF" with best by date of 05/27/2026 printed at the top of the bag.
The product subject to the public heath alert bears establishment number "EST. 13051" inside the USDA mark of inspection. The item was shipped to a Schnucks distribution center in Missouri and was further distributed to store locations in Illinois, Indiana, Missouri, and Wisconsin.
The problem was discovered when the establishment notified FSIS that their sole consignee received a consumer complaint of ravioli product in a bag labeled as tortellini.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers' freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Jessica Fazio, Plant Manager of P. E. & F, Inc., at (314) 645‑6239 ext. 230, or by email at jessica@faziosbakery.com.
WASHINGTON, July 27, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ham salad products containing Food and Drug Administration (FDA) regulated breadcrumb products that have been recalled by Newly Weds Foods, due to concerns that the products may be contaminated with Listeria monocytogenes (Lm). FSIS is issuing this public health alert to ensure that consumers are aware that these products, which bear the USDA mark of inspection, should not be consumed. As more information becomes available, FSIS will update this public health alert. Consumers should check back frequently because additional products may be added.
The following products subject to the public health alert are [view labels]:
12-oz. printed plastic tubs containing “RESER’S FINE FOODS Ham Salad” with sell by dates of 09/01/25.
5-lb. clear plastic tubs containing “Molly’s Kitchen Ham Salad” with sell by dates of 08/31/25.
The problem was discovered when Reser’s Fine Foods, Inc., a Topeka, Kan., establishment, determined that they used FDA-regulated breadcrumb products subject to an FDA recall because the breadcrumbs may be contaminated with Lm.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumption of food contaminated with Lm can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS is concerned that some product may be in consumers’ or retailers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. Retailers that have purchased these products are urged not to serve or sell them. These products should be thrown away or returned to the place of purchase.
WASHINGTON, July 11, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for pulled pork products due to misbranding and undeclared allergens. The two ready-to-eat products barbecue pulled pork and pulled pork burrito filling are prepared with Worchester sauce, which contains soy, a known allergen that is not declared on the product labels. The pulled pork burrito filling product also contains anchovies and egg whites, known allergens that are not declared on the product label. Consumers with allergies to soy, fish or egg should not consume these products. A recall was not requested because the products are no longer available for purchase.
The ready-to-eat pulled pork and burrito filling products were produced between April 3, 2025, and July 9, 2025. The following products are subject to the public health alert [view labels]:
16-oz. plastic trays containing “Prep Chef PULLED PORK WITH BBQ SAUCE” with “Best if used by” dates 7/10/25, 7/15/25, 7/24/25, or 7/31/25 and lot codes 025148, 025153, 5162, 5169, 5176, 5189, or 5190 printed on the label.
10-lb. boxes containing two 5-lb. bags of frozen “Prep Chef BBQ PULLED PORK & GOUDA MAC AND CHEESE BURRITO FILLING” with USE BY dates 4/3/2026, 4/24/2026, 5/2/2026, 5/5/2026, 5/16/2026, 5/22/2026, 6/12/2026, 6/23/2026 or 7/3/2026 and lot codes 025093, 025114, 025122, 025136, 025142, 5163, 5171, or 5184 printed on the side of the box.
The products subject to the public heath alert bear establishment number “EST. 46046” inside the USDA mark of inspection. The barbecue pulled pork product was shipped to Hannaford grocery store locations in Maine and New York. The pulled pork burrito filling product was distributed to Jacksons gas station locations in Idaho for breakfast burrito products.
The problem was discovered during a routine FSIS label review.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact feedback@rothbrands.com.
WASHINGTON, July 02, 2025 – The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS), is issuing a public health alert for ready-to-eat (RTE) beef jerky stick products that may be contaminated with extraneous materials, specifically plastic. FSIS did not request a recall because the affected products are no longer available for purchase.
The RTE beef jerky stick products were produced on May 27, 2025 and have an 18-month shelf life. The following products subject to the public health alert are [view labels]:
6.9 oz. bags containing six 1.15-oz. vacuum-sealed packages containing of "RIVERBEND RANCH Original Beef Stick" with a "Best By date of 11/27/2026"
6.9 oz. bags containing six 1.15 oz. vacuum-sealed packages containing of "RIVERBEND RANCH Jalapeño Beef Stick" with a "Best By date of 11/27/2026"
The products bear "EST. 47282" on the back of the label. These items were shipped to a company that further distributed the products online and to locations nationwide, including Puerto Rico.
The problem was discovered after the firm notified FSIS that it received consumer complaints reporting transparent pieces of plastic in the beef stick products.
There have been no confirmed reports of injury or illness due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers' pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Top Notch Jerky, LLC at 208‑372‑3231 or QATopNotch2020@gmail.com.
WASHINGTON, June 20, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for meat sauce products produced without the benefit of federal inspection. The producer, Thompson’s Spanish Sauce Manufacturing, LLC, in Marion, Ind., does not have a federal grant of inspection. FSIS is issuing a public health alert because the company was unavailable to confirm their actions to remove affected products from commerce. FSIS will continue to work with the company and conduct effectiveness checks to verify customers are notified and ensure no affected products are available to consumers.
The following meat sauce products are subject to the public health alert [view labels]:
16-oz. jars of “Thompson's B-K Spanish Sauce.”
16-oz. jars of “Thompson's B-K Spicey Coney Sauce.”
These products do not bear the USDA mark of inspection. The items were sold to distribution and retail locations in Illinois and Indiana, and were further distributed to certain farmers’ markets.
The problem was discovered during routine FSIS surveillance activities at a retail location in Roann, Ind., where FSIS investigators identified these thermally-processed meat sauce products for sale without a federal mark of inspection.
There have been no confirmed reports of illness due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators, freezers, or pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away.
Consumers and members of the media with questions about the public health alert can contact Michael Thompson, owner, Thompson’s Spanish Sauce Manufacturing, LLC, at mikeyts@icloud.com.
WASHINGTON, June 3, 2025 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for ground beef products that may be contaminated with E. coli O157:H7. FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The raw ground beef item was produced on May 22, 2025, and May 23, 2025. The following product is subject to the public health alert [view labels]:
1-lb. vacuum-packed packages of "ORGANIC RANCHER ORGANIC GROUND BEEF 85% LEAN 15% FAT" with "Use or Freeze By 06‑19‑25" and "Use or Freeze By 06‑20‑25" as represented on the packaging.
The product bears establishment number "EST. 4027" inside the USDA mark of inspection. This item was shipped to distributor locations in Connecticut, Georgia, Illinois and Maryland and was further distributed to Whole Foods Market retail locations nationwide.
The problem was discovered when the establishment notified FSIS that they shipped into commerce ground beef product that tested positive for E. coli O157:H7.
There have been no confirmed reports of illness due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
E. coli O157:H7 is a potentially deadly bacterium that can cause dehydration, bloody diarrhea and abdominal cramps 2–8 days (3–4 days, on average) after exposure the organism. While most people recover within a week, some develop a type of kidney failure called hemolytic uremic syndrome (HUS). This condition can occur among persons of any age but is most common in children under 5-years old and older adults. It is marked by easy bruising, pallor, and decreased urine output. Persons who experience these symptoms should seek emergency medical care immediately.
FSIS is concerned that some product may be in consumers' refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume ground beef that has been cooked to a temperature of 160 F. The only way to confirm that ground beef is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, https://www.fsis.usda.gov/safetempchart.
Media and consumers with questions regarding the public health alert can contact Danny Desautels, NPC Processing, Inc., President, at 802‑660‑0496 (office), 802‑310‑7644 (cell) or ddesautels@npcprocessing.com.
WASHINGTON, June 2, 2025 – The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for a frozen not-ready-to-eat ham croquette product due to misbranding and undeclared allergens. The product contains soy and sesame, known allergens, which are not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to soy and sesame are aware that this product should not be consumed. A recall was not requested because the affected product is no longer available for purchase.
The frozen not-ready-to-eat ham croquette item was produced on various dates in April and May 2025. The following product is subject to the public health alert [view labels]:
1.96-lb. boxes containing "HAM CROQUETTES Las que si tienen el sabor cubano A TASTE OF CUBA CROQUETAS DE JAMÓN" with expiration dates of "November 2025," "December 2025" and "January 2026" printed on the boxes.
The product bears establishment number "EST. 2725" inside the USDA mark of inspection. This item was shipped to distributor locations in Florida.
The problem was discovered during routine FSIS in-plant labeling verification activities. The establishment used a different breadcrumb ingredient than normally used.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an adverse reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers' freezers. Consumers who have purchased this product are urged not to consume it. The product should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Hernesto Aguirre, Owner, at croquetaslamary@gmail.com.
Editor’s Note: May 23, 2025 – Distribution and company contact information have been updated.
WASHINGTON, May 22, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) chicken soup products due to misbranding and an undeclared allergen. The products contain wheat, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to wheat are aware that these products should not be consumed. A recall was not requested because the affected products are no longer available for purchase.
The RTE chicken soup items were produced on April 10, 2025. The following products are subject to the public health alert [view labels]:
24-oz. plastic cups labeled “Signature SELECT Creamy Chicken & Wild Rice SOUP with White Meat Chicken” on the lid and labeled “Signature SELECT Chicken Corn CHOWDER with White Meat Chicken Smoke Flavor Added” on the side of the cup with a “BEST BY June 24 25” and lot code “8225 5100” printed on the bottom of the cup.
The products bear establishment number “P-46381” inside the USDA mark of inspection. These items were shipped to retail and distributor locations nationwide.
The problem was discovered by a retailer after a store employee identified “Signature SELECT Creamy Chicken & Wild Rice SOUP with White Meat Chicken” product bearing the correct top label but incorrect side label. The retailer reported the issue to the producing establishment, and the establishment notified FSIS.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
FSIS is concerned that some products may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to serve, sell, or consume them. These products should be thrown away or returned to the place of purchase.
Consumers with questions should contact Albertsons Companies’ Customer Service Center at 1‑877‑723‑3929 Monday through Friday from 5 a.m. to 9 p.m. PST. Media with questions regarding the public health alert can contact Albertsons Media Relations at media@albertsons.com.
WASHINGTON, May 13, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) chicken and bacon wrap products due to concerns that the products may be contaminated with Listeria monocytogenes. A recall was not requested because the affected products are no longer available for purchase.
The ready-to-eat (RTE) chicken and bacon ranch wrap products were produced on May 2, 2025. The following products subject to the public health alert are [view labels]:
10-oz. clear plastic clamshell packages containing “Big Y quick easy meals CHICKEN BACON RANCH WRAP” with “Sell By 05/07/2025” and lot code 25122.
10-oz. clear plastic clamshell packages containing “MARKET 32 BY PRICE CHOPPER Chicken Bacon Ranch Wrap” with “Sell Through 05/07/2025” and lot code 25122.
The products bear establishment number “P34657” inside the USDA mark of inspection. These items were shipped to distributors in Massachusetts and New York and further distributed to retail locations in Connecticut, Massachusetts and New York.
The problem was discovered when a state public health partner notified FSIS of a product sample that tested positive for Listeria monocytogenes.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS is concerned that some products may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Mike Pepin, Vice President of Operations, Rachael's Food Corp., at 413‑888‑1629.
WASHINGTON, May 1, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for potato chip products containing chicharrón (pork cracklings) that were imported from the Republic of Colombia. Colombia is ineligible to export meat products to the United States. FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The mixed bags of potato chips containing chicharrón were imported between August 2024 and March 2025. The following products are subject to the public health alert, regardless of the product date [view labels]:
270-g. plastic bag containing six 45-g. foil bags of “De Todito NATURAL” mixed chips with “CHICHARRÓN AMERICANO JACKS,” “Margarita,” and “NATU CHIPS.”
165-g. foil bags containing “De Todito NATURAL” mixed chips with “CHICHARRÓN AMERICANO JACKS,” “Margarita,” and “NATU CHIPS.”
270-g. plastic bag containing six 45-g. foil bags of “De Todito BBQ” mixed chips with “CHICHARRÓN AMERICANO JACKS,” “Margarita,” and “NatuChips.”
165-g. foil bags containing “De Todito BBQ” mixed chips with “CHICHARRÓN AMERICANO JACKS,” “Margarita,” and “NatuChips.”
165-g. foil bags containing “De Todito LIMÓN” mixed chips with “CHICHARRÓN AMERICANO JACKS,” “Margarita,” “TOSTITOS,” and “NATU CHIPS.”
270-g. plastic bag containing six 45-g. foil bags of “De Todito LIMÓN” mixed chips with “CHICHARRÓN AMERICANO JACKS,” “Margarita,” “TOSTITOS,” and “NATU CHIPS.”
140-g. foil bags containing “GOLPE CON TODO SABOR LIMÓN” mixed chips with “RIZADAS,” “PLÁTANOS,” and “Chicharrón Fred.”
The products subject to the public health alert do not bear any import marks on the labels. These items were shipped to distributors in Florida and New York and to retail locations nationwide.
The problem was discovered when FSIS was performing routine surveillance activities at two retailers and found meat products from Colombia that are not eligible to be exported to the U.S.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
FSIS is concerned that some products may be in consumers’ pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Jack Wilson, Owner, LatinFood US at 631‑681‑5276 or jwilson@latinfoodus.com.
WASHINGTON, May 1, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for retail ground beef products sold by Bismillah Halal Meats, a retail market in Marietta, Ga., that may be contaminated with E. coli O103. FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The raw ground beef was produced and sold directly to consumers from April 10‑23, 2025. All products were weighed, wrapped, and labeled in-store at the time of purchase. All ground beef products produced and sold by this retailer from April 10‑23, 2025, are subject to this public health alert.
The products do not bear an establishment number or the USDA mark of inspection because they were produced under retail exemption.
The problem was discovered when a sample was collected and analyzed by FSIS during retail surveillance and the sampling results showed the presence of E. coli O103. There have been no confirmed reports of illness due to consumption of these products.
E. coli O103 is a Shiga-toxin producing E. coli (STEC). Many clinical laboratories do not test for non-O157 STEC, such as O103, because it is harder to identify than STEC O157:H7. People can become ill from STECs 2–8 days (average of 3–4 days) after consuming the organism.
Most people infected with STEC O103 develop diarrhea (often bloody) and vomiting. Some illnesses last longer and can be more severe. Infection is usually diagnosed by testing a stool sample. Vigorous rehydration and other supportive care are the usual treatment; antibiotic treatment is generally not recommended. Most people recover within a week, but, rarely, some develop a more severe infection. Hemolytic uremic syndrome (HUS), a type of kidney failure, is uncommon with STEC O103 infection. HUS can occur in people of any age, but it is most common in children under 5 years old, older adults and people with weakened immune systems. It is marked by easy bruising, pallor and decreased urine output. People who experience these symptoms should seek emergency medical care immediately.
FSIS is concerned that some products may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Murad ManJiyani, Bismillah Halal Meats, Owner, at 404‑786‑1356 or muradmanji@gmail.com.
WASHINGTON, April 19, 2025 – The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for pork carnitas products that may be contaminated with foreign material, specifically pieces of metal. FSIS did not request a recall because this product is no longer available for sale in commerce.
The fully cooked pork carnitas products were produced from April 1‑2, 2025. The following products are subject to the public health alert [view labels]:
16-oz. sleeved tray packages containing "Pork Carnitas SEASONED & SEARED PORK WITH JUICES SLOW COOKED WITH CITRUS" with "USE BY" dates "06/30/2025" or "07/01/2025" printed on the side of the packaging.
The products subject to the public health alert bear establishment number "Est. 46049" inside the USDA mark of inspection. These items were shipped to Aldi supermarkets nationwide.
The problem was discovered when the establishment notified FSIS that during routine process checks they found equipment damage that may have contaminated the carnitas products with pieces of metal.
There have been no confirmed reports of injury due to consumption of these products. Anyone concerned about an injury should contact a healthcare provider.
Although this product is no longer available for sale, FSIS is concerned that some product may be in consumers' refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Members of the media with questions about the public health alert can contact Chuck Miller, Cargill Meat Solutions, at media@cargill.com. Consumers can contact Cargill's Consumer Hotline at 1‑844‑419‑1574.
WASHINGTON, April 11, 2025 – The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for various soup and bowl products that may be contaminated with foreign material, specifically wood, in an FDA-regulated ingredient, cilantro.
The following products are subject to the public health alert [view products & labels]:
These items were shipped to retail and institutional locations in Illinois, Indiana, Michigan, and Ohio. FSIS anticipates that other products may be added, which could result in nationwide impacts.
The problem was discovered when an FSIS establishment notified FSIS that an FDA-regulated ingredient was recalled for foreign material.
FSIS is concerned that some product may be in consumers' and institutional refrigerators or freezers. Consumers who have purchased these products are urged not to consume them and institutions are urged not to serve the products. These products should be thrown away or returned to the place of purchase.
Media and consumers should check this release frequently on the FSIS website as additional products may be added.
WASHINGTON, March 31, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for a ready-to-eat (RTE) white chicken chili imported from Canada that did not receive the benefit of import reinspection. A recall was not requested because the product is no longer available for purchase.
The following product is subject to the public health alert [view labels]:
7 lbs. 2 oz. cartons containing eight, 14.3-oz. plastic tubs of “Allen FAMILY FOODS WHITE CHICKEN CHILI with Bell Peppers, Corn & White Beans,” with lot codes E225077, E225079, E225080, E225081, E225083 and “best before by dates” of 03/18/2026, 03/20/2026, 03/21/2026, 3/22/2026, and 03/24/2026.
The product bears the Canadian establishment seal “7011.” This item was shipped to select Costco stores in Idaho, Oregon and Washington.
The problem was discovered by FSIS inspection personnel who determined that the chicken chili product was not presented for FSIS import reinspection.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Billy Allen, Director of Operations, Allen Family Foods at 1‑877‑813‑1884 or email at customercare@allenfamilyfoods.ca.
WASHINGTON, Feb. 12, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for frozen, fully cooked ready-to-eat (RTE) meat and poultry pasties due to misbranding and an undeclared allergen. The products were produced using an egg wash, which contains egg, a known allergen, that is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to eggs are aware that this product should not be consumed. A recall was not requested because the affected products are no longer available for purchase.
The frozen, fully cooked ready-to-eat (RTE) meat and poultry pasties were produced on and prior to December 11, 2024, and have a one-year shelf-life. The following products are subject to the public health alert [view labels]:
8-oz. plastic packages containing “The Pasty Oven Pasty WITH CHICKEN & CHEESE” with best by dates of December 11, 2025, and prior.
8-oz. plastic packages containing “The Pasty Oven Pasty PIZZA PASTY WITH PEPPERONI” with best by dates of December 11, 2025, and prior.
15-lb. cases containing 30 8-oz. units of “The Pasty Oven Pasty WITH CHICKEN & CHEESE” with best by dates of December 11, 2025, and prior.
15-lb. cases containing 30 8-oz. units of “The Pasty Oven Pasty PIZZA PASTY WITH PEPPERONI” with best by dates of December 11, 2025, and prior.
The products bear establishment number “EST. 20650” inside the USDA mark of inspection. These items were sold at the establishment’s restaurant in Michigan and shipped to fundraiser groups, such as those for schools and non-profit organizations, in Michigan, Minnesota, and Wisconsin. However, the product was not served at schools and is not part of the food provided by the USDA for the National School Lunch Program.
FSIS discovered the problem during routine labeling review activities when it found that the egg ingredient was not listed on the final product label.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Gene Carollo, Pasty Oven, Inc., President, at gcarollo@uplogon.com and Karen Secinaro, Manager, at pastys.factory@gmail.com.
WASHINGTON, Jan. 27, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for frozen, fully cooked Wegmans breaded chicken breast nuggets that may be contaminated with extraneous material, specifically bone fragments. FSIS is issuing this public health alert to ensure that consumers are aware that this product should not be consumed. A recall was not requested because the product is no longer available for purchase.
The frozen, fully cooked breaded chicken breast nugget product was produced on August 26, 2024. The following product is subject to the public health alert [view labels]:
46-oz. plastic packages containing “Wegmans FAMILY PACK FULLY COOKED Breaded Chicken Breast with Rib Meat” and a best if used by date 08 26 25, located on the back of the packaging next to the barcode in the lower right corner.
The product subject to the public health alert bears establishment number “P-33944” inside the USDA mark of inspection. This item was produced solely for Wegmans Food Markets and distributed to retail locations in Delaware, Maryland, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania, Virginia, and Washington, D.C.
FSIS was notified of the issue after Wegmans received multiple consumer complaints of bone fragments in the frozen fully cooked breaded chicken breast nugget product.
There have been no confirmed reports of injury due to consumption of these products. Anyone concerned about an injury should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased this product are urged not to consume it. This product should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Wegmans Food Markets at 1‑855‑934‑3663 Monday through Friday from 8:00 a.m. - 7:00 p.m. or Saturday and Sunday from 8:00 a.m. - 5:00 p.m. ET.
WASHINGTON, Jan. 8, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for frozen product labeled as Chicken Curry Empanadas due to misbranding and an undeclared allergen. The product labeled as Chicken Curry Empanadas may actually contain Apple Cinnamon Empanadas, which contain milk, a known allergen, that is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to milk are aware that this product should not be consumed. A recall was not requested because the affected product is no longer available for purchase.
The frozen empanada products labeled as Chicken Curry Empanadas that may contain Apple Cinnamon Empanada products were produced on November 14, 2024, and packaged on November 20, 2024, and November 21, 2024. The following product is subject to the public health alert [view label]:
9.6-oz. cardboard packages labeled as “bettergoods TRADITIONALLY CRAFTED Chicken Curry Empanadas” with “BEST BY: 05/21/26” or “BEST BY: 05/22/26” and “EST. P33967” on the side of the box.
The products bear establishment number “P33967” on the side of the box. These items were shipped to Walmart locations nationwide.
The problem was discovered when the producing establishment notified FSIS that its distributor received four consumer complaints indicating that the apple cinnamon empanada product was packaged inside the chicken curry empanada retail packaging.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Members of the media and consumers with questions regarding the public health alert can contact Sanjiv Mody, President of Rajbhog Foods, at 551‑222‑4700 or sanjivmody@rajbhog.com.
WASHINGTON, Jan. 5, 2025 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns of frozen, raw ground beef products that may be contaminated with foreign material, specifically hard plastic and metal. FSIS is issuing this public health alert to ensure that consumers are aware that this product should not be consumed. A recall was not requested because the product is no longer available for purchase.
The frozen, raw ground beef items were produced on December 10, 2024. The following product is subject to the public health alert [view label]:
vacuum-sealed packages weighing approximately one pound containing “Turner Farm”, “STOCKYARDS PACKING COMPANY GROUND BEEF” and lot code 241210.
The product bears establishment number “EST. M2035” inside the USDA mark of inspection. The product was shipped to one retail location at Turner Farm, 7400 Given Road, Cincinnati, Ohio, 45243.
The problem was discovered after the firm notified FSIS that it received a consumer complaint reporting that pieces of hard plastic and metal were found in the raw ground beef product.
There have been no confirmed reports of injury or illness due to consumption of this product. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Andy Korb, Owner, Stockyards Packing Co. LLC at 513‑312‑0648 or andy.korb@theyardsOH.com.
WASHINGTON, Dec. 4, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) frozen chicken products that did not receive the benefit of import reinspection. A recall was not requested because the products are no longer available for purchase.
The following products subject to the public health alert are [view labels]:
5-lb. cardboard box packages containing “yummy Dino Buddies Holiday NUGGETS Breaded nugget shaped white meat chicken patties” with a “Best if Used by Date” of 11/06/26 and Lot #241556.
The products bear the Canadian establishment seal “348.” These items were shipped to one Costco retail location at 7095 Marketplace Dr, Goleta, California, 93117.
The problem was discovered by FSIS inspection personnel who determined that the products were not presented for FSIS import reinspection.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media with questions regarding the public health alert can contact Andrea Staub, Senior Vice President Corporate Communications, Maxi Canada, Inc., at 410‑341‑2755 or Andreas@maxi.com. Consumers with questions regarding the public health alert can contact Maxi Consumer Care at 866‑866‑6164.
WASHINGTON, Dec. 2, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for frozen ready-to-eat pork mortadella products that may have been illegally imported from Ecuador, a country ineligible to export meat and poultry products to the United States. FSIS is continuing to investigate the origins of this product, and there may be additional products affected.
The following products subject to the public health alert are [view labels]:
1-lb. vacuum-sealed packages containing “Mortadela ESPECIAL BOLOGNIA.
The products subject to the public health alert do not bear an establishment number or the USDA mark of inspection. These items were shipped to retail and distributor locations in Connecticut, Massachusetts, Maryland, New Jersey, New York, Pennsylvania, and Rhode Island.
The problem was discovered when FSIS was performing surveillance activities at a warehouse and found mortadella bologna products that did not have the USDA mark of inspection.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Veronica Vasquez, firm President, Ecuatorianita Imports & Exports, LLC, at 732‑309‑0183 or ecuaimports1@hotmail.com.
WASHINGTON, Nov. 22, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for beef tallow products that were illegally imported from Mexico and are ineligible for entry into the United States. The products were not certified for export to the U.S. by the government of Mexico as being produced under equivalent inspection, they do not identify a certified establishment number on their packaging, and they were not presented to FSIS for import reinspection as required. These factors make the products ineligible to import into the U.S. and unfit for human consumption. FSIS is continuing to investigate how these products entered the country.
The following products are subject to the public health alert, regardless of the product date [view labels]:
1-kg or 500-g bag packages containing “INCA GRASA COMESTIBLE DE SEBO BOVINO” (edible fat from beef tallow).
The products subject to the public health alert do not bear an establishment number nor a USDA mark of inspection. These items were shipped to distribution and retail locations in Arizona.
The problem was discovered when FSIS was performing surveillance activities at a retailer and found beef tallow products from an unverified supplier in Mexico and, therefore, ineligible for import into the United States.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ pantries or on retailers’ shelves. Retailers who have purchased the products are urged not to sell them. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Jose Gallardo, Owner, MEXDIS, LLC, at 520‑455‑7239 or mexdisllc20@gmail.com.
WASHINGTON, Oct. 24, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for various meat and poultry products that were illegally imported from the Republic of the Union of Myanmar. FSIS is continuing to investigate how these products entered the country.
The following products are subject to the public health alert, regardless of the product date. View labels in Burmese.
180-g. cans containing “BEST BEEF CURRY.”
425-g. cans containing “BEST Chicken Biryani.”
360-g. cans containing “Hti Mi Gwik Dry MoHinGa Paste.”
425-g. cans containing “BEST Myanmar Duck Blood.”
400-g. cans containing “Eain Chak MoHinGa Paste.”
160-g. vacuum sealed clear packages containing “Min Thar Gyi Dried Fish.”
400-g. cans containing “Eain Chak Coconut Soup Paste.”
The products subject to the public health alert do not bear an establishment number nor a USDA mark of inspection. These items were shipped to retail locations in Arizona, California, Iowa, Kansas, Maryland, Minnesota, Nebraska, Oklahoma, and Texas.
The problem was discovered when FSIS was performing surveillance activities at a retailer and found meat and poultry products from Myanmar that are not eligible to be exported to the U.S.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers' pantries and on retailers' shelves. Retailers who have purchased the products are urged not to sell them. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Leo Chen, Managing Member, at 480‑399‑6811 or Leo251185@gmail.com.
WASHINGTON, Oct. 8, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for chicken salad products labeled as Cranberry Chicken Salad due to misbranding and undeclared allergens. The product labeled as Cranberry Chicken Salad may actually contain Classic Chicken Salad, which contains wheat, a known allergen, that is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to wheat are aware that this product should not be consumed. A recall was not requested because the affected product is no longer available for purchase.
The Classic Chicken Salad labeled as Cranberry Chicken Salad was produced on September 30, 2024. The following products are subject to the public health alert [view labels]:
12-oz. clear plastic packages containing “Cranberry Chicken Salad with white meat chicken” with a use-by date of 10/25/24.
The products subject to the public health alert bear establishment number “P-7573” printed on the top of the product label. These items were shipped to retail locations in Connecticut, Massachusetts, Rhode Island, New Jersey, and New York.
The problem was discovered when the establishment notified FSIS that it received a customer complaint that packages labeled as Cranberry Chicken Salad contained Classic Chicken Salad.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Members of the media with questions about the public health alert can contact Ricardo Alvarez, CEO, Hans Kissle, at 978‑556‑4500 Ext 215 or ralvarez@hanskissle.com. Consumers with questions can contact Katie Hatch, Customer Service Representative, Hans Kissle, at 978‑556‑4500 or customercomplaints@hanskissle.com.
WASHINGTON, Aug. 16, 2024 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for various meat and poultry products that were illegally imported from the Republic of the Union of Myanmar. Myanmar is a country ineligible to export meat and poultry products to the United States. FSIS is continuing to investigate how these products entered the country.
The products and labels in the attached list are subject to the public health alert, regardless of the product date. View labels [here].
The products subject to the public health alert do not bear any import marks on the labels. These items were shipped to retail locations nationwide.
The problem was discovered when FSIS was performing routine surveillance activities at a retailer and found meat and poultry products from Myanmar that are not eligible to be exported to the U.S.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers' pantries and on retailers' shelves. Retailers who have purchased the products are urged not to sell them. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Pyae Phyo Thandar, Sales Manager at Hong Sar, LLC - Hinthar Inc., at 317‑701‑4039 or kinghongsar@gmail.com.
WASHINGTON, July 10, 2024 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat meat and poultry products that were illegally imported from the Philippines. The Philippines is a country not eligible to export meat and poultry products to the United States. FSIS is continuing to investigate how these products entered the country.
The following products are subject to the public health alert, regardless of the product date [view labels]:
150-g. can of "Argentina BRAND CORNED BEEF."
175-g. can of "Argentina BRAND CORNED BEEF."
260-g. can of "Argentina BRAND CORNED BEEF."
150-g. can of "PUREFOODS CORNED BEEF."
210-g. can of "PUREFOODS CORNED BEEF."
150-g. can of "CHUNKEE CORNED BEEF."
190-g. can of "CHUNKEE CORNED BEEF."
7.43-oz. jar of "Lady's Choice Chicken Spread."
The products subject to the public health alert do not bear any producing establishment information. These items were shipped to restaurant and retail locations in Connecticut, Delaware, Maryland, New Jersey, New York, North Carolina, Ohio, South Carolina, and Virginia.
The problem was discovered when FSIS was performing routine surveillance activities at a retailer and found meat and poultry products from the Philippines that are not eligible to be exported to the U.S.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers' and restaurants' pantries and on retailers' shelves. Retailers who have purchased the products are urged not to sell them. Consumers and restaurants who have purchased these products are urged not to consume or serve them. Consumers are asked to double bag the product when discarding it to reduce the possibility of animals accessing the product because USDA cannot confirm whether the products were properly heated to control pathogens of concern to domestic livestock and poultry.
Consumers and members of the media with questions about the public health alert can contact John Ducar, Owner, Redsealuxury, LLC, at 646‑669‑4020 or johnny@redsealux.com.
WASHINGTON, June 12, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for not-ready-to-eat pork and beef bacon products due to levels of sodium nitrite that exceed the regulatory limit. FSIS is issuing this public health alert to ensure that consumers are aware that this product should not be consumed. A recall was not requested because the affected product is no longer available for purchase.
The dry cured pork and beef bacon items were produced between April 12, 2024, and May 31, 2024. The following products are subject to the public health alert [view labels]:
Packages purchased by weight at the retail counter containing “FARMSTEAD LOCAL HOUSE SMOKED BACON,” bearing sell by dates MAY.2.24 through JUN.27.24.
Packages purchased by weight at the retail counter containing “FARMSTEAD BUTCHER BLOCK BUCK BOARD BACON,” bearing sell by dates MAY.2.24 through JUN.27.24.
Packages purchased by weight at the retail counter containing “FARMSTEAD BUTCHER BLOCK PORK JOWL WHOLE HOUSE SMOKED,” bearing sell by dates MAY.2.24 through JUN.27.24.
Packages purchased by weight at the retail counter containing “FARMSTEAD BUTCHER BLOCK HOUSE SMOKED BEEF BACON,” bearing sell by dates MAY.2.24 through JUN.27.24.
Approximately 1 pound packages containing “Clark Farms Smoked Pork Jowl Bacon,” bearing lot code H130RH.
Approximately 1 pound packages containing “Clark Farms Smoked Pork Bacon,” bearing lot code H130RH.
Approximately 1 pound packages containing “Clark Farms Smoked Pork Shoulder Bacon,” bearing lot code H130RH.
Approximately 1 pound packages containing “Farmstead Butcher Block Smoked Pork Jowl Bacon,” bearing lot code H81AB.
Approximately 1 pound packages containing “Farmstead Butcher Block Smoked Pork Bacon,” bearing lot code H81AB.
Approximately 1 pound packages containing “Southwinds Cattle Company Smoked Beef Belly Bacon,” bearing lot code B237AB.
Some of products subject to the public health alert bear establishment number “EST. 47852” inside the USDA mark of inspection. These items were shipped to farmers markets and farm stores in Kentucky and Tennessee as well as direct-to-consumer sales. The other items sold by various weight were purchased from the retail counter at Farmstead Butcher Block. Other products were produced under a custom exemption and do not bear the USDA mark of inspection.
The problem was discovered by FSIS while performing routine inspection activities. FSIS discovered that the establishment’s formulation of sodium nitrite, a restricted ingredient, exceeded the regulatory limit.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Farmstead Butcher Block at 270‑200‑4224 or office@mmmbutcherblock.com.
WASHINGTON, June 10, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for a salad product labeled as Bistro Grande Southwestern Style with Chicken due to misbranding and undeclared allergens. The salad product labeled as Southwestern Style with Chicken may actually contain Chicken Caesar Salad containing wheat and fish (anchovies), known allergens, which are not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to wheat and fish are aware that this product should not be consumed. A recall was not requested because the affected product is no longer available for purchase.
The salad bowls were packaged on May 28, 2024. The following product is subject to the public health alert [view labels]:
11.75-oz. bowls containing “Bistro GRANDE SOUTHWESTERN STYLE WITH CHICKEN WITH SALSA RANCH Dressing” with use by date “JUN 12 2024,” time stamp “08:59,” lot code “217638176,” and establishment number “P-27497” printed on the label.
These items were shipped to retail locations in California and Nevada.
The problem was discovered when the producing establishment notified FSIS that it received a consumer complaint that a salad product labeled as Bistro Grande Southwestern Style with Chicken contained Chicken Caesar Salad.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers with questions about the public health alert can contact customer service for Ready Pac Food, Inc., at 800‑800‑7822 or bfa-consumer.affairs@bonduelle.com. Members of the media with questions about the public health alert can email bfa-newsroom@bonduelle.com.
WASHINGTON, June 7, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for product labeled as bao Thai-style curry chicken due to misbranding and undeclared allergens. The product labeled as bao curry chicken may actually contain teriyaki chicken bao products, which contain soy and sesame, known allergens, which are not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to soy and sesame are aware that this product should not be consumed. A recall was not requested because the affected product is no longer available for purchase.
The fully cooked, frozen bao curry chicken product was packaged on March 20, 2024. The following product is subject to the public health alert [view labels]:
10-oz. boxes containing four “WOW BAO BAO THAI-STYLE CURRY CHICKEN” with “best if used by” date “4/12/25” printed on the side of the box.
The product bears establishment number “P-40001” inside the USDA mark of inspection. These items were shipped to Walmart retail locations nationwide.
The problem was discovered when the producing establishment notified FSIS that it received a consumer complaint that a box labeled bao Thai-style curry chicken contained pouches of the bao teriyaki chicken.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers with questions about the public health alert can contact Brandon Tammaro, VP Strategic Growth, Wow Bao, at 888‑496‑9226 or contactus@wowbao.com. Members of the media with questions about the public health alert can contact Brett Stein, General Manager, Brett Anthony Foods at 847‑272‑4309 or b.stein@brettanthonyfoods.com.
WASHINGTON, May. 2, 2024 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns of raw pork chorizo products that may be contaminated with a foreign material, specifically hard plastic and metal. FSIS is issuing a public health alert to ensure that consumers are aware that this product should not be consumed. A recall was not requested because the product is no longer available for purchase.
The raw pork chorizo items were produced on February 12, 2024. The following product is subject to the public health alert [view labels]:
12-oz. vacuum-sealed packages containing "LEAN apco BRAND MEATS ALL NATURAL PREMIUM CHORIZO" with the best-by date of 5/12/24.
The product bears the establishment number "EST. 602" inside the USDA mark of inspection. The product was distributed to H-E-B grocery stores in Texas.
The problem was discovered after the firm notified FSIS that it had received a consumer complaint reporting that pieces of hard plastic and metal were found in the raw pork chorizo product.
There have been no confirmed reports of injury or illness due to consumption of this product. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers' refrigerators or freezers. Consumers who have purchased this product are urged not to consume them. This product should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact David Roe, Operations Manager, San Antonio Packing Company at 210‑224‑5441 or Operations@realchorizo.com.
WASHINGTON, April 20, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ground beef products that may be contaminated with E. coli O157:H7. FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The raw ground beef items were produced on March 28, 2024. The products have a “Use/Freeze by” date of April 22, 2024, and packaging date of “032824.” The list of products that are subject to the public health alert can be found here. The labels for these products can be found on the FSIS website [view labels].
The products subject to the public health alert bear establishment number “EST. 960A” inside the USDA mark of inspection. These items were shipped to food service institutions and retail locations nationwide.
The problem was discovered by the establishment while conducting an inventory of product that was on hold because it was found positive for E. coli O157:H7. The company notified FSIS that they inadvertently used a portion of the contaminated beef to produce ground beef products that they subsequently shipped into commerce.
There have been no confirmed reports of illness due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
E. coli O157:H7 is a potentially deadly bacterium that can cause dehydration, bloody diarrhea and abdominal cramps 2–8 days (3–4 days, on average) after exposure the organism. While most people recover within a week, some develop a type of kidney failure called hemolytic uremic syndrome (HUS). This condition can occur among persons of any age but is most common in children under 5-years old and older adults. It is marked by easy bruising, pallor, and decreased urine output. Persons who experience these symptoms should seek emergency medical care immediately.
FSIS is concerned that some product may be in consumers’ and food service institutions’ freezers. Consumers who have purchased these products are urged not to consume them and food service institutions are urged not to serve these products. These products should be thrown away or returned to the place of purchase.
FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume ground beef that has been cooked to a temperature of 160 F. The only way to confirm that ground beef is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, https://www.fsis.usda.gov/safetempchart.
Consumers and members of the media with questions about the public health alert can contact Gina Adami, Greater Omaha Packing Co., Inc. Representative, at 402‑575‑4702 or gadami@gmail.com.
WASHINGTON, March. 21, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for imported frozen Siluriformes products that were illegally imported from the People’s Republic of China and are ineligible for entry into the United States. The products were not certified for export to the U.S. by the government of China as being produced under equivalent inspection, they do not identify a certified establishment number on their packaging, and they were not presented to FSIS for import reinspection as required. These factors make the products ineligible to import into the U.S. and unfit for human consumption. FSIS is working with other agencies to investigate how these products entered the country.
The following product is subject to the public health alert [view labels]:
12-oz. (340 g) plastic packages containing “FROZEN STRIPED PANGASIUS MAWS.”
The products subject to the public health alert do not bear any producing establishment information or import marks on the labels and are packed in plain white shipping cartons devoid of labels or markings. These items are believed to have been shipped to retail and wholesale locations in New York, Oklahoma, and Pennsylvania.
The problem was discovered during FSIS surveillance activities conducted at a wholesaler. By law, commercial imports of meat, poultry, and egg products must be produced in certified establishments in eligible countries, and these products must be presented to FSIS for import reinspection prior to entering U.S. commerce. Raw Siluriformes fish products from specific establishments in China are eligible for importation provided the raw materials originate from a certified establishment (Eligible Foreign Establishments – China (usda.gov)).
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in retailers’ and consumers’ freezers or refrigerators. Retailers who have purchased the products are urged not to sell them. Consumers who purchased the products should not consume them and need to dispose of them properly. Consumers are asked to dispose of the products by double bagging them to reduce the possibility of animals accessing the products.
Media and consumers with questions regarding the public health alert can contact Susie Yang, Accountant, Fuxin USA Inc at 347‑881‑9899 or fuxinusa@gmail.com.
WASHINGTON, Feb. 27, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for Nurture Life’s Chicken Parm with Super Veggie Spaghetti meal products due to misbranding and an undeclared allergen. The product’s spaghetti component contains egg white, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with an allergy to egg are aware that this product should not be consumed. A recall was not requested because the affected product is no longer available for purchase.
The fully cooked, not shelf-stable chicken meals were produced between Dec. 27, 2023, and Feb. 20, 2024. The following product is subject to the public health alert [view labels]:
5.9-oz. tray with sleeve label containing “nurture life KIDS MEALS CHICKEN PARM WITH SUPER VEGGIE SPAGHETTI” with “enjoy by” dates ranging from Jan. 9, 2024, to March 1, 2024.
The chicken meal packaging does not have a USDA mark of inspection. These items were sold online and shipped directly to consumers nationwide.
The problem was discovered when FSIS was notified that the firm discovered that egg was not declared on the label during an internal audit.
There have been no confirmed reports of adverse reactions due to consumption of this product. Anyone concerned about an illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased this product are urged not to consume it. These products should be thrown away or returned to the place of purchase.
Members of the media with questions about this public health alert can contact Frank Chen, Chief Marketing Officer, Nurture Life, Inc., at 312‑517‑1888 or email at fchen@nurturelife.com. Consumers with questions about this public health alert can contact Jennifer Chow, Co-Founder, Nurture Life, Inc., at 312‑517‑1888 or email at jchow@nurturelife.com.
Editor’s Note: Feb. 9, 2024 – Details of this public health alert were updated to reflect additional products affected by the dairy products that have been recalled due to possible Listeria Monocytogenes contamination. Check back frequently to see if additional products have been added.
WASHINGTON, Feb. 8, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for meat and poultry products containing Food and Drug Administration (FDA) regulated dairy products that have been recalled by Rizo-Lopez Foods, due to concerns that the products may be contaminated with Listeria monocytogenes. FSIS is issuing this public health alert to ensure that consumers are aware that these products, which bear the USDA mark of inspection, should not be consumed. As more information becomes available, FSIS will update this public health alert. Consumers should check back frequently because additional products may be added.
The list of products subject to the public health alert are available here, including information the establishment numbers and states where the products were distributed. The labels are available here.
The problem was discovered when the establishments notified FSIS that they used FDA-regulated dairy products that may be contaminated with Listeria monocytogenes to produce the poultry products. FDA is continuing its investigation into the dairy products produced by Rizo-Lopez Foods.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS is concerned that some product may be in consumers’ or retailers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. Retailers that have purchased these products are urged not to serve or sell them. These products should be thrown away or returned to the place of purchase.
WASHINGTON, Feb. 7, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns of a frozen ready-to-eat (RTE) chicken pilaf product that may be contaminated with foreign material, specifically rocks. FSIS is issuing this public health alert to ensure that consumers are aware that this product should not be consumed. A recall was not requested because the product is no longer available for purchase.
The frozen RTE chicken, lentil, and caramelized onion pilaf product was produced on various dates from November 1, 2023, through January 19, 2024. The following product is subject to the public health alert [view labels]:
14-oz. plastic packages containing “Trader Joe’s Chicken, Lentil, & Caramelized Onion Pilaf WITH SAFFRON BASMATI RICE, DARK CHICKEN MEAT, DATES & GOLDEN RAISINS.”
The product bears the establishment number “P-45322” inside of the USDA mark of inspection. The product was distributed to Trader Joe’s grocery stores nationwide.
The problem was discovered when the establishment notified FSIS that it received multiple consumer complaints of rocks in the chicken pilaf. One consumer reported a dental injury from consuming the product.
FSIS has received no additional reports of injury or illness from consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased this product are urged not to consume them. This product should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can call the producing establishment, Mama Vicky’s, at 818‑583‑0003.
WASHINGTON, Jan. 18, 2024 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert out of an abundance of caution due to concerns about Salmonella illnesses that may be associated with ready-to-eat (RTE) charcuterie meat products in Busseto brand Charcuterie Sampler and Fratelli Beretta brand Antipasto Gran Beretta.
The Fratelli Beretta brand Antipasto Gran Beretta was sold at Costco in a 24-oz. twin-pack (two 12-oz. trays). The Busseto brand Charcuterie Sampler was sold at Sam's Club in an 18-oz. twin-pack (two 9-oz. trays). Any lot code associated with either product is potentially contaminated. The products are no longer available for purchase at Costco and Sam's Club.
The products of concern bear establishment number "EST. 7543B" and/or "EST. #47967" inside the USDA mark of inspection or printed on the package. Label images can be found in the Centers for Disease Control and Prevention (CDC) Food Safety Alert.
FSIS has been working with the CDC and state public health partners to investigate a multistate outbreak of 47 Salmonella I 4:i:- illnesses in 22 states with onset dates ranging from November 20, 2023, through January 1, 2024. In the ongoing outbreak investigation, the state of Minnesota identified the outbreak strain from an unopened Busseto brand charcuterie sampler, which led to recall 01‑2024 on January 3, 2024. FSIS will continue the investigation and issue new information as it becomes available.
Consumption of food contaminated with Salmonella can cause salmonellosis, one of the most common bacterial foodborne illnesses. The most common symptoms of salmonellosis are diarrhea, abdominal cramps, and fever within 6 hours to 6 days after eating the contaminated product. The illness usually lasts 4 to 7 days. Most people recover without treatment. In some persons, however, the diarrhea may be so severe that the patient needs to be hospitalized. Older adults, infants, and persons with weakened immune systems are more likely to develop a severe illness. Individuals concerned about an illness should contact their health care provider.
FSIS is concerned that some product may be in consumers' refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media with questions regarding the public health alert can contact Marco Lastrico, Public Relations, Busseto Foods, at 917‑634‑1685 or m.lastrico@barabinousa.com. Consumers with questions regarding the public health alert can contact the Busseto Recall Hotline at 866‑552‑4916.
WASHINGTON, Jan. 18, 2024 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert because Dim Sum Factory Inc., a Flushing, N.Y., establishment, produced and distributed raw, frozen pork dumpling products without the benefit of federal inspection. A recall was not requested because the products are no longer available for purchase.
The raw, frozen pork wonton dumpling products were produced on various dates since September 6, 2023, and have a shelf life of 18 months. The following product is subject to the public health alert [view label]:
1.5-lb. vacuum-packed packages containing "GOGO DUMPLING Pork & Shepherd's Purse Wontons (Handmade)."
The products bear establishment number "EST. 1656" inside the USDA mark of inspection. These items were shipped to a distributor in New York and sold online nationwide.
The problem was discovered during routine FSIS surveillance activities. FSIS determined that the location where the pork wonton products were being produced were not on the official premises of the establishment and, therefore, were not inspected.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers' freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Daisy Ching, Sales Manager of Dim Sum Factory Inc., at 862‑872‑0076.
Editor’s Note: April 5, 2024 – Details of this public health alert were updated to reflect additional misbranded products that were produced and distributed. The distribution area was also expanded to include retail locations in Michigan.
WASHINGTON, Jan. 5, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for frozen mushroom risotto products due to misbranding and an undeclared allergen. The product labeled as porcini mushroom risotto bites may actually contain hot dogs in puff pastry, which contain sesame, a known allergen, that is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with an allergy to sesame are aware that these products should not be consumed. A recall was not requested because the product is no longer available for purchase.
The frozen Porcini Mushroom Risotto Bites packages, which may actually contain hot dogs in puff pastry, were produced April 11, 2023, and Dec. 27, 2023. The following products are subject to the public health alert [view labels]:
7.5-oz. cardboard packages labeled as “Wild Fork Porcini Mushroom Risotto Bites” with lot code 101231, “BEST BY DATE: 10/11/2024”, and EST. 39896 on the side of the box.
7.5-oz. cardboard packages labeled as “Wild Fork Porcini Mushroom Risotto Bites” with lot code 361231, “BEST BY DATE: 6/27/2025,” and EST. 32068 on the side of the box.
The products bear establishment number “EST. 39896” or “EST. 32068” on the side of the box. There is no USDA mark of inspection. These items were shipped to retail locations in California, Florida, Illinois, Maryland, Massachusetts, Michigan, New Jersey, New York, Pennsylvania, Texas, and Wisconsin.
The problem was discovered after the firm notified the U.S. Food and Drug Administration (FDA) that it had received a consumer complaint reporting that the hot dogs in puff pastry product had been found in a package labeled as mushroom risotto bites. FDA then notified FSIS about the issue. Additional products were discovered that fall within the scope of this public health alert after the establishment received one customer complaint and notified FSIS.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Jessica Levitzki, Director of Food Safety & Compliance, The Fillo Factory, at 201‑439‑1036 ext. 22 or jessica@fillofactory.com.
WASHINGTON, Dec. 7, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) product labeled as birria-inspired beef soup due to misbranding and an undeclared allergen. The product labeled as birria-inspired beef soup may actually contain plant-based chicken noodle soup, which contains sesame, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The RTE product labeled as birria-inspired beef soup that may contain plant-based chicken noodle soup were produced on November 18, 2023. The following product is subject to the public health alert [view label]:
24-oz. plastic cups labeled “WHOLE FOODS MARKET KITCHENS Birria-Inspired Beef Soup with Hominy” with “USE BY 01/02/24” and lot code 11183. The top of the plastic cups may be labeled “WHOLE FOODS MARKET KITCHENS Plant-Based Chicken Noodle Soup MADE WITH PLANT-BASED PROTEIN. DOES NOT CONTAIN CHICKEN.”
The product subject to the public health alert bears the establishment number “EST. 18235” inside the USDA mark of inspection. These items were shipped to retail locations in Arizona, California, Hawaii, Idaho, Montana, Nevada, Oregon, and Washington.
The issue was discovered by the retailer after a store employee identified a case of RTE Plant-Based Chicken Noodle Soup product bearing the correct top label but incorrect front and back labels. The retailer reported the issue to the producing establishment, and the establishment notified FSIS.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Members of the media with questions regarding the public health alert can contact Andrew Hearns, EVP of Quality and Food Safety of Kettle Cuisine, at 617‑409‑1100 or ahearns@kettlecuisine.com. Consumers with questions can contact Paul Nazario, Director of Retail Sales at Kettle Cuisine, at 360‑931‑1494 or pnazario@kettlecuisine.com.
WASHINGTON, Nov. 17, 2023 - The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for meat and poultry jerky products due to misbranding and undeclared allergen. The product may contain soy, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers are aware that this product should not be consumed. A recall was not requested because the product is no longer available for purchase.
The meat and poultry jerky items were produced on various dates from Sep. 21 through Nov. 9, 2023. The following products are subject to the public health alert [view labels]:
1.75-oz., 2.75-oz., and 8-oz. packages containing “Pruski’s Market Spicy Beef Jerky” and a “SELL BY” date ranging from 03/21/24 through 05/09/24 represented on the back of the packages.
1.75-oz., 2.75-oz., and 8-oz. packages containing “Pruski’s Market Beef Jerky” and a “SELL BY” date ranging from 03/21/24 through 05/09/24 represented on the back of the packages.
1.75-oz, 2.75-oz., and 8-oz. packages containing “Pruski’s Market Turkey Jerky” and a “SELL BY” date ranging from 03/21/24 through 05/09/24 represented on the back of the packages.
3-oz. packages containing “HOOSER CUSTOM MEATS BEEF JERKY MESQUITE SMOKED” and a “SELL BY” of 04/23/24 represented on the back of the packages.
Packages purchased by weight at the retail counter, containing “Beef Jerky Regular”, “Spicy Beef Jerky”, or “Turkey Jerky” with Pack Date ranging from 9/21/23 through 11/9/23.
Some of the products subject to the Public Health Alert bear establishment number “EST.19908” inside the USDA mark of inspection. These items were shipped to retail locations in Texas. The other jerky items sold by various weight were purchased from the retail counter at Pruski’s Market in Texas and do not bear the establishment number or the mark of inspection on the label.
The problem was discovered by FSIS inspection personnel during a verification task where they discovered that soy was not included on the label.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some products may be in consumers’ pantries or refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the recall can contact Edmund Pruski, Owner, Pruski’s Market at 210‑649‑2151 or pruskismarket@yahoo.com.
WASHINGTON, Oct. 6, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for a ready-to-eat (RTE) stuffed pepper soup with meatballs product due to misbranding and undeclared allergen. The product contains egg, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers are aware that this product should not be consumed. A recall was not requested because the product is no longer available for purchase.
The RTE stuffed pepper soup with meatballs product was produced on Sept. 28, 2023. The following product is subject to the public health alert [view labels]:
32-oz. clear cups of “R KITCHEN Stuffed Pepper Soup with Meatballs” with a Best By: 11/27/23 date and lot code 048480 printed on the lid.
The product bear establishment number “EST. 18019” inside the USDA mark of inspection. This item was shipped to retail locations in Massachusetts.
The problem was discovered during a label review by the establishment.
There have been no confirmed reports of adverse reactions due to consumption of this product. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased this product are urged not to consume it. This product should be thrown away or returned to the place of purchase.
Media with questions regarding the public health alert can contact Michael Jolly, Marketing Manager, at 978‑970‑3832 or mfjolly@plenus-group.com. Consumers with questions regarding the public health alert can contact Krystian Madrid, Quality Control and Assurance Director, at 978‑970‑3832 or kmadrid@plenus-group.com.
WASHINGTON, Oct. 6, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that ready-to-eat (RTE) ham products produced by Sunnyvalley Smoked Meats, a Manteca, Calif. establishment, may be contaminated with Listeria monocytogenes. A recall was not requested because it is believed that the affected products are no longer in commerce.
The RTE ham products were produced on Sept. 25, 2023. The following product is subject to the public health alert [view labels]:
4-lb. (average weight) vacuum-packed clear plastic packages containing “Kirkland Signature Applewood Smoked MASTER CARVE HALF HAM Boneless With Natural Juices” with Use / Freeze by date Jan 20 24 and a sticker with lot number 264 - 4.
The products bear establishment number “EST. 17823” inside the USDA mark of inspection. These items were shipped to retail locations in California and Nevada.
The problem was discovered after the establishment’s laboratory testing indicated the product may be contaminated with Listeria monocytogenes. The establishment notified FSIS that some of the affected product was distributed into commerce.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media with questions regarding the public health alert can contact Nikki Richardson, at 918‑521‑0531 or nikki.richardson@jbssa.com. Consumers with questions regarding the public health alert can contact Courteney Rangel, Quality Assurance Manager, at 209‑647‑3504 or crangel@sunnyvalleysmokedmeats.com.
WASHINGTON, Sept. 16, 2023 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for canned meat product due to under processing. FSIS is issuing this public health alert to ensure that consumers are aware that this product should not be consumed. A recall was not requested because it is believed that the product is no longer available for consumers to purchase.
The canned meat item was produced by Hormel Foods Corp. Services, LLC, an Austin, Minn. establishment, on Aug. 17, 2023. The following product is subject to the public health alert [view labels]:
12-oz. metal cans containing "SPAM Classic" with "BEST BY AUG 2026" date and lot code A08173 printed on the bottom of the can.
The product bears establishment number "EST. 199" inside the USDA mark of inspection. The product involved in this alert was shipped to H.E.B. retail locations in Texas; no other retailers are involved in this alert.
The problem was discovered when the firm reported that they inadvertently shipped product that may not have been adequately processed to reach commercial sterility.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers' pantries or refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
Consumers with questions about this PHA can contact Hormel Foods' Consumer Engagement Team at 1‑800‑523‑4635 or cresponse@hormel.com. Members of the media with questions about this PHA can contact Hormel Foods' Public Relations Group at 507‑437‑5611 or media@hormel.com.
WASHINGTON, Sept. 13, 2023 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for a ready-to-eat (RTE) Kirkland Signature chicken tortilla soup product due to misbranding. The label declares the product as gluten-free, a false negative claim. FSIS is issuing this public health alert to ensure that consumers with reactions to gluten are aware that these products should not be consumed. A recall was not requested because the affected products are no longer available for purchase.
The ready-to-eat chicken tortilla soup items were produced on July 26, 2023. The following products are subject to the public health alert [view labels]:
2-lb. tubs containing "KIRKLAND Signature CHICKEN TORTILLA SOUP WITH WHITE CHICKEN MEAT" with "USE BY: 11/23/23" and lot code 1394066 printed on the side of the cup just below the lip.
The products bear establishment number "P-18468" inside the USDA mark of inspection. These items were shipped to retail locations in Alaska, California, Idaho, Montana, Nevada, Oregon, Utah, and Washington.
The problem was discovered when the establishment notified FSIS that laboratory testing found gluten in the chicken tortilla soup, which is labeled as gluten-free.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers' refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Members of the media with questions regarding the public health alert can contact Andrew Hearns, EVP of Quality and Food Safety at Kettle Cuisine, at 617‑409‑1100 or ahearns@kettlecuisine.com. Consumers with questions can contact Jacqui Valerio, Customer Relationship Manager at Kettle Cuisine, at 619‑409‑1100 or jvalerio@kettlecuisine.com .
WASHINGTON, Aug. 25, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for Wegmans Jamaican Jerk-style, raw, marinated chicken products due to misbranding and undeclared allergens. The marinade in the chicken products may contain milk, soy, and wheat, known allergens, which are not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to milk, soy, and wheat are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The raw, Jamaican Jerk-style chicken products were produced on August 16, 2023. The following products are subject to the public health alert [view labels]:
1-lb. vacuum-packed plastic packages containing “Wegmans jamaican jerk style Chicken Thighs” with a use by date of “9/6/23.”
1-lb. vacuum-packed plastic packages containing “Wegmans jamaican jerk style Chicken Breast Cutlets” with a use by date of “9/6/23.”
The products subject to the public health alert bear the establishment number “EST. P-7567” inside the USDA mark of inspection. These items were shipped to retail locations in Massachusetts, New York, and Pennsylvania.
The problem was discovered when the establishment notified FSIS that it identified an equipment malfunction that may have led to potential cross-contamination with milk, soy, and wheat, known allergens, which are not declared on the product labels.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some products may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions regarding the public health alert can contact Wegmans Customer Care at 1‑800‑934‑6267.
WASHINGTON, Aug. 25, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for fresh, fully cooked, ready-to-eat (RTE) ShopRite brand chicken noodle soup products due to misbranding and undeclared allergens. The product labeled as chicken noodle soup may actually contain Italian-style wedding soup, which contains milk, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The fresh, fully cooked, RTE Italian-style wedding soup products labeled as chicken noodle soup were produced on August 8, 2023. The following product is subject to the public health alert [view label]:
20-oz. plastic cups labeled “A SHOPRITE BRAND bowl & basket CHICKEN NOODLE soup” with a use by date of “09/23/23.”
The product subject to the public health alert bears the establishment number “EST. P-18468” inside the USDA mark of inspection. These items were shipped to retail locations in New Jersey and New York.
The problem was discovered when the establishment notified FSIS that a retail store employee who was stocking refrigerated store shelves found soups labeled as chicken noodle and Italian-style wedding soup in the same shipping box. The retailer reported the issue to the producing establishment.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Members of the media with questions regarding the public health alert can contact Andrew Hearns, EVP of Quality and Food Safety of Kettle Cuisine, at 617‑409‑1100 or ahearns@kettlecuisine.com. Consumers with questions can contact Jacqui Valerio, Customer Relationship Manager at Kettle Cuisine, at 619‑409‑1100 or jvalerio@kettlecuisine.com.
WASHINGTON, Aug. 7, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that ready-to-eat (RTE) salads and wraps with meat and poultry may contain contaminated lettuce. The lettuce, which is regulated by the Food and Drug Administration (FDA), may be contaminated with deer feces. FSIS is issuing this public health alert to ensure that consumers are aware that this product should not be consumed.
The RTE salad and wrap products were produced on August 1, 2023, and August 2, 2023. The following products subject to the public health alert are [view labels]:
8.65-oz. plastic film packages containing “Chicken Caesar Wrap FRESH SEASONS Kitchen” with lot code 21323 and 21423 and Sell by dates of 8/9/2023 and 8/10/2023.
7.2-oz. plastic film packages containing “Chicken Caesar Wrap FRESH SEASONS Kitchen” with lot code 21323 and Fresh Thru date of 8/10/2023.
8.5-oz. plastic clam shell packages containing “Chicken Caesar Salad FRESH SEASONS Kitchen” with lot code 21323 and Fresh Thru date of 8/9/2023.
8.55-oz. plastic clam shell packages containing “Chef Salad FRESH SEASONS Kitchen” with lot codes 21323 and 21423 and Sell by dates of 8/9/2023 and 8/10/2023.
5.85-oz. plastic clam shell packages containing “Bacon, Lettuce and Tomato Salad FRESH SEASONS Kitchen” with lot codes 21323 and 21423 and Sell by dates of 8/9/2023 and 8/10/2023.
The products bear the establishment number “P-45091” or “Est. 45091” on the front label. The products were shipped to retail locations in Minnesota and Wisconsin.
The problem was discovered when an FSIS-regulated establishment notified FSIS that its supplier of FDA-regulated lettuce is conducting a recall because the lettuce may be contaminated with deer feces.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
Media and consumers with questions regarding the public health alert can contact Jill Teut, Senior Director of Communications, Taher, Inc., at (952) 345‑2873 or communications@taher.com.
WASHINGTON, Aug. 4, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns of a raw beef product that may be contaminated with extraneous material, specifically soft, clear plastic. FSIS is issuing this public health alert to ensure that consumers are aware that this product should not be consumed. A recall was not requested because the product is no longer available for purchase.
The raw beef item was produced on July 25, 2023. The following product is subject to the public health alert [view labels]:
Approximately 1.5-lb. plastic tray packages containing “USDA CHOICE BLACK ANGUS BEEF FROM ALDI, BEEF FOR CARNE PICADA” with a “Use or Freeze by” date of Aug. 22, 2023, Julian Date 206, and time stamp between 08:43 through 09:23.
The product bears the establishment number Est. 85M on the back label. The product was available in select ALDI grocery stores nationwide.
The problem was discovered when the establishment notified FSIS that it received a complaint from a retail store that soft, clear plastic was noticed in the product.
There have been no confirmed reports of injury or illness due to consumption of this product. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased this product are urged not to consume them. This product should be thrown away or returned to the place of purchase.
Consumers with questions about the public health alert can call Cargill at 844‑419‑1574. Members of the media with questions can contact April Nelson, Cargill, at 952‑913‑5466.
WASHINGTON, July 19, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for Never Any! brand ready-to-eat (RTE) ham and cheese lunch kits containing chocolate chip cookies that may contain peanut, a known allergen, which is not declared on the finished product label. FSIS is issuing this public health alert to ensure that consumers with an allergy to peanut are aware that this product should not be consumed. A recall was not requested because the products are believed to no longer be available for purchase.
The ham and cheese lunch kits with the chocolate chip cookies were produced between June 27, 2023, and July 5, 2023. The following products are subject to the public health alert [view labels]:
2.9-oz. plastic tray packages containing “NEVER ANY! UNCURED HAM & CHEESE LUNCH KIT” with a Use By date of “SEPT 18 2023”.
The products subject to the public health alert bear establishment number “645” inside the Canadian mark of inspection. These items were shipped to retail locations nationwide.
The problem was discovered when the producing establishment was notified by their chocolate chip cookie supplier that the chocolate chip cookies may contain peanut residue, a known allergen, which is not declared on the label. The producing establishment then notified FSIS that the cookies were used in products distributed to the United States.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers with a peanut allergy who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers with questions about the public health alert can contact Maple Leaf Foods Inc. at 1‑877‑526‑4520. Members of the media who have questions can contact Maple Leaf Foods Inc. at media.hotline@mapleleaf.com.
WASHINGTON, May 2, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that frozen ready-to-cook meatloaf entrée products may contain undeclared milk, a known allergen. These entrees are removed from their master carton and delivered to consumers in ready to prepare trays that do not bear an ingredient statement. While egg, soy, and wheat are declared in the ingredient list that appears on the carton, milk is not. FSIS is issuing this public health alert to ensure that consumers with allergies to egg, milk, soy, and wheat are aware that these products should not be consumed. A recall was not requested because the products are no longer available for distribution to consumers.
This item was produced on February 1, 2023, February 13, 2023, March 15, 2023, and March 28, 2023. The following product is subject to the public health alert [view labels]:
14-oz. paper or plastic three compartment tray with a sealed plastic cover containing “MEATLOAF & TOMATO SAUCE MIXED RICE AND SPINACH” and a use or discard by date of “May 1, 2023, May 13, 2023, June 15, 2023, and June 28, 2023.”
These items were shipped to organizations serving the senior population in Southern California and were further distributed through home-delivery meal service programs.
The problem was discovered by FSIS during a routine label verification task. FSIS inspectors observed that the meatloaf contained milk, but the establishment did not list milk as an ingredient on the case label. The individual trays delivered to consumers do not include an ingredient statement. Consumers should be aware that in addition to milk, this product also contains the allergens egg, soy, and wheat.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some products may be in consumers’ freezers. Consumers with allergies to egg, milk, soy and wheat who have received these products are urged not to consume them. These products should be thrown away or returned to the meal service program.
Consumers with questions about the public health alert can contact Robert Cavanagh, President, Langlois Frozen Foods, at 949‑497‑4739 or robert.cavanagh@langloisfoods.com. Members of the media with questions about the public health alert can contact Michael Cavanagh, Operations Manager, Langlois Frozen Foods, at 949‑497‑4739 or mikecavanagh@langloisfoods.com.
WASHINGTON, April 25, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that ready-to-eat meat soup products may have been prepared, packed, or held under insanitary conditions, which may result in the product spoiling prematurely. FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The following products are subject to the public health alert [view labels]:
48-oz. packages containing two 24-oz. cups of “Ivar’s PUGET SOUND CLAM CHOWDER WITH BACON” with Use By dates 4/26/2023, 4/27/2023, 5/3/2023, 5/4/2023, 5/5/2023, 5/11/2023, 5/23/2023, 5/30/2023, 6/2/2023, 6/6/2023, 6/7/2023, 7/5/2023, 7/20/2023, 8/1/2023, 8/10/2023, and 8/17/2023.
48-oz. packages containing two 24-oz. cups of “Ivar’s Loaded Baked Potato Soup” with Use By dates 5/9/2023, 5/19/2023, 6/16/2023, and 7/18/2023.
48-oz. packages containing two 24-oz. cups of “Ivar’s Rustic Zuppa Toscana Italian Sausage and Vegetable Soup” with Use By dates 4/30/2023, 5/2/2023, 5/14/2023, 5/15/2023, 5/21/2023, 5/22/2023, and 5/30/2023.
20-oz. cup of “Ivar’s PUGET SOUND Clam Chowder WITH BACON” with Use By dates 4/26/2023, 5/5/2023, 6/6/2023, 7/20/2023, and 8/10/2023.
20-oz. cup of “PIKE PLACE FISH MARKET WORLD FAMOUS CLAM CHOWDER WITH BACON” with Use By dates 5/4/2023, 7/5/2023, and 8/1/2023.
The products bear establishment number “EST. 20173” inside the USDA mark of inspection. These items were shipped to retail locations nationwide and exported to Mexico.
The problem was discovered when the establishment notified FSIS that they had received multiple consumer complaints regarding bloated soup packages. Upon further review, the establishment found that some product spoiled prematurely. The establishment’s lab testing of the prematurely spoiled products found high levels of spoilage bacteria in the products.
There have been no confirmed reports of illness due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumption of food contaminated with spoilage organisms can cause illness in immunocompromised individuals.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media with questions regarding the public health alert can contact Bob Donegan, President, Ivar’s Soup Company, at bobd@keepclam.com. Consumers with questions regarding the public health alert can contact Robert Green, Director of Technical Services, Ivar’s Soup Company, at robertg@keepclam.com.
WASHINGTON, April 7, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) fresh salad products with chicken and ham that contain Food and Drug Administration (FDA) regulated lettuce that has been recalled for possible Listeria monocytogenes (Lm) contamination.
FSIS is issuing this public health alert to ensure that consumers are aware that this product should not be consumed.
The fresh salads with chicken and ham were produced on various dates from March 10, 2023, through March 24, 2023. The following products subject to the public health alert are [view labels]:
5.5-oz. clear plastic packages containing “Fruit Ridge Farms White Chicken Caesar Salad” with sell by dates 03/10/23 through 04/14/23.
4.6-oz. clear plastic packages containing “Fruit Ridge Farms Chef Salad with Ham” with sell by dates 03/10/23 through 04/14/23.
5.5-oz. clear plastic packages containing “BELL’S BISTRO White Chicken Caesar Salad” with sell by dates 03/10/23 through 04/14/23.
4.6-oz. clear plastic packages containing “BELL’S BISTRO Chef Salad with Ham” with sell by dates 03/10/23 through 04/14/23.
The products bear establishment number “EST. 17050” or “P-17050” inside the USDA mark of inspection. These items were shipped to retail locations in Illinois, Indiana, Kentucky, Michigan, Ohio, Tennessee, and Wisconsin.
The problem was discovered when the firm notified FSIS that they used FDA-recalled lettuce to produce the fresh salad with chicken and ham products.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS is concerned that some products may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Alicia Richards, Food Safety & Quality Manager at 616‑399‑7084 Ext. 416 or arichards@russrestaurants.com.
WASHINGTON, March 10, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that fully cooked, ready-to-eat (RTE) chicken salad product may contain cashews a known allergen, which is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The fully cooked, RTE chicken salad products were produced on March 4, 2023. The following products subject to the public health alert are [view label]:
12-oz. clear plastic trays containing “TRADER JOE’S Wine Country WHITE CHICKEN SALAD WITH Cranberries & Pecans.” with a best by date of 3/12/2023.
The products subject to the public health alert bear establishment number “P-34834” inside the USDA mark of inspection. The product was shipped to retail locations in Idaho, Oregon, and Washington.
The problem was discovered when the firm notified FSIS that it received a consumer complaint that cashews were found in the chicken salad product.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers with questions regarding the public health alert can contact Taylor Farms at Customercare@taylorfarms.com or 855‑455‑0098. Media with questions regarding the public health alert can contact Taylor Farms at press@taylorfarms.com.
WASHINGTON, Feb. 23, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that fully cooked, ready-to-eat (RTE) pasta sauce labeled as pizza sauce contains anchovies and milk, known allergens, as well as ground beef and sulfites, which are not declared on the product label. FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The fully cooked, RTE pasta sauce items labeled as pizza sauce were produced on January 25, 2023. The following products subject to the public health alert are [view label]:
16-oz. tub containing “NEW SEASONS BRIGHT & FLAVORFUL HOMESTYLE PIZZA SAUCE with slow-simmered plum tomatoes” with a best if used by date of “3/26/23.”
The product subject to the public health alert does not bear a USDA establishment number or mark of inspection. These items were shipped to retail locations in Oregon and Washington.
The problem was discovered after the firm received a consumer complaint that meat was in the pizza sauce and notified FSIS. The establishment determined that employees labeled a limited number of “Bolognese Pasta Sauce” packages as “Homestyle Pizza Sauce”.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Lana Slezak, Executive Vice President/Founder of Heritage Specialty Foods, LLC, at 503‑252‑1545.
WASHINGTON, Feb. 15, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that not-ready-to-eat meat products were subject to temperature abuse during storage at a distribution center prior to delivery to retailers, which may have resulted in the growth of spoilage organisms or pathogens. FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The following products are subject to the public health alert [view labels]:
7-oz. cardboard box packages containing “Signature SELECT BREAKFAST BOWL SAUSAGE POTATOES, EGGS, SAUSAGE & CHEDDAR CHEESE” with a best if used by date of JAN 11 24, lot code S011322 and UPC 21130 18044.
7-oz. cardboard box packages containing “Signature SELECT BREAKFAST BOWL BACON POTATOES, EGGS, BACON & CHEDDAR CHEESE” with a best if used by date of JAN 16 24, lot code S016331 and UPC 21130 18043.
7-oz. cardboard box packages containing “Signature SELECT BREAKFAST BOWL MEAT LOVERS POTATOES, EGGS, CHEDDAR CHEESE, SAUSAGE & BACON” with a best if used by date of JAN 11 24, lot code S011322 and UPC 21130 18042.
7-oz. cardboard box packages containing “Signature SELECT BREAKFAST BOWL SAUSAGE & GRAVY POTATOES, COUNTRY STYLE GRAVY, EGGS, SAUSAGE & CHEDDAR CHEESE” with a best if used by date of JAN 11 24, lot code S011331 and UPC 21130 18045.
The products bear establishment number “EST 45210” on the top panel of the cardboard box. These items were shipped to Albertsons Companies retail locations in Northern California and Northern Nevada. The Signature Select Breakfast Bowl products were available for purchase at the following Albertsons Companies banner stores: Andronico’s Community Markets, Pak ‘N Save, Safeway and Vons.
The problem was discovered when the producing establishment notified FSIS that their customer reported storing the product in an unrefrigerated area. FSIS found that the product was held at an incorrect temperature and then shipped into commerce. All remaining inventory of the affected items have been removed from the stores and destroyed.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions regarding the public health alert can contact Albertsons Companies Customer Service Center at 1‑877‑723‑3929, which is available Monday through Friday 5 a.m. to 9 p.m. Pacific Time.
WASHINGTON, Feb. 14, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that the raw, ready-to-cook chicken entrée products may be missing labeling that includes the list of ingredients and cooking instructions. This product contains soy and milk, known allergens, which may not be declared on the finished product label. FSIS is issuing this public health alert to ensure that consumers with an allergy to soy and dairy are aware that these products should not be consumed and to ensure that consumers properly cook this product to an internal temperature of 165 degrees as measured by a food thermometer. A recall was not requested because the products are no longer available for purchase.
The raw, ready-to-cook chicken entrée products were produced on February 3, 2023. The following products are subject to the public health alert [view labels]:
12-oz. plastic wrapped metal containers containing “aprons READY TO COOK MEAL FOR ONE SUN-DRIED TOMATO & CHEESE-STUFFED CHICKEN WITH LEMON-GARLIC POTATOES” with a use by date of 02/15/2023.
The products bear establishment number “P-48176” inside the USDA mark of inspection. These items were shipped to Publix distribution locations in Florida, Georgia and North Carolina.
The problem was discovered when the establishment notified FSIS that the product was inadvertently misbranded when a printer did not place the bottom label on the product packaging. As a result, the list of ingredients and the cooking instructions are missing.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume chicken that has been cooked to a temperature of 165 F. The only way to confirm that chicken is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, https://www.fsis.usda.gov/safetempchart.
Consumers and members of the media with questions regarding the public health alert can contact John Miller, Director of Operations, Tampa Bay Fisheries at 813‑752‑8883 ext. 202 or johnm@tbfish.com
WASHINGTON, Feb. 8, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that the ready-to-eat (RTE) pork sausage link products may contain milk, a known allergen, which is not declared on the finished product label. FSIS is issuing this public health alert to ensure that consumers with an allergy to dairy are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The smoked pork Linguica link products were produced on various dates between January 8, 2021, and February 6, 2023. The following products are subject to the public health alert [view labels]:
Plastic vacuum-wrapped packages containing “GOULART’S Smoked LINGUICA LINKS (wine & smoke flavor added).”
Plastic vacuum-wrapped packages containing “GOULART’S Smoked LINGUICA LINKS HOT (wine & smoke flavor added).”
The products bear establishment number “EST. 8262” inside the USDA mark of inspection. These items were sold through retail sales in California.
The problem was discovered during routine inspection activities when FSIS observed the establishment adding nonfat dry milk to an ingredient in the Linguica links products. The finished product labels for these Linguica links products do not identify nonfat dry milk as an ingredient and do not declare milk as an allergen.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some products may be in consumers’ refrigerators or freezers. Consumers with a dairy allergy who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Antonio Caetano, owner of Goulart’s Sausage Co., at 408‑279- 8130.
WASHINGTON, Feb. 3, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for frozen chicken products due to misbranding and an undeclared allergen. The product contains cashews, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to cashews are aware that these products should not be consumed. A recall was not requested because it is believed that the products are no longer available for consumers to purchase.
The frozen products are labeled as Chicken Korma with Basmati Turmeric Rice but may contain Vegetable Tikka Masala with Turmeric Rice. This item was produced on November 8, 2022. The following product is subject to the public health alert [view labels]:
10-oz. containers of “Wegmans Chicken Korma with Basmati Turmeric Rice” with Best By 08 NOV 2023.
The products subject to the public health alert bear establishment number “P-34641” inside the USDA mark of inspection. These items were shipped to retail locations in New York and Pennsylvania.
The problem was discovered when the producing establishment notified FSIS that they received consumer complaints reporting that product labeled as chicken korma actually contained vegetable tikka masala. The vegetable tikka masala contains cashews not declared on the chicken korma product label.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Giovanni Gomez, Director of Business Development, Cafe Spice, at 845‑863‑0910 or Giovanni@cafespice.com.
WASHINGTON, February 3, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) stuffed chicken product because the product may not be fully cooked due to underprocessing. FSIS is issuing this public health alert to ensure that consumers are aware that this product should not be consumed. A recall was not requested because the product is no longer available for consumers to purchase.
The RTE broccoli stuffed chicken breast product was produced by Vanguard Culinary Group, LTD, a Fayetteville, N.C. establishment, on December 3, 2022. The following product is subject to the public health alert [view labels]:
16 oz (1 lb.) vacuum sealed trays containing “PARK STREET DELI Broccoli Stuffed Chicken BONELESS SKINLESS CHICKEN BREAST HAND STUFFED WITH BROCCOLI & CHEDDAR AU GRATIN” with a use by date of 1/30/2023.
The product subject to this public health alert bears establishment number “P-8334” inside the USDA mark of inspection. This item was shipped to retail locations in Alabama, Florida, New York, Pennsylvania, and Virginia.
The problem was discovered when consumers reported to FSIS that the product labeled as fully cooked appeared to be raw.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Jeff Gruber, Vice President of Food Safety and Quality Assurance at Vanguard Culinary Group, LTD, at jeffgruber@vanguardculinary.com and 910‑364‑6804.
WASHINGTON, Feb. 1, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) meat snack products containing Food and Drug Administration (FDA) regulated chocolate wafers that have been recalled due to an undeclared allergen, specifically peanut residue. FSIS is issuing this public health alert to ensure that consumers are aware that this product should not be consumed.
The meat snack items were produced with the recalled chocolate wafers on various dates from January 2, 2023, through January 18, 2023. The following products are subject to the public health alert [view labels]:
2.71-oz. plastic tray packages containing “PRIVATE SELECTION SNACK BOARD SMOKED DRY CURED RED WINE SALAMI” with lot code 11110900408 and Best By dates of “APR 10 2023” and “APR 18 2023”.
3-oz. plastic tray packages containing “GREENFIELD NATURAL MEAT CO. SMOKED UNCURED PEPPERONI” with lot code 63100268821 and Best By date “APR 03 2023”.
2.9-oz. plastic tray packages containing “PRIVATE SELECTION SNACK BOARD SMOKED DRY CURED SPICY CALABRESE SALAMI” and lot code 11110605471 with Best By date of “APR 03 2023”and “APR 19 2023”.
The products subject to the public health alert bear establishment number “645” inside the Canadian mark of inspection. These items were shipped to retail locations nationwide.
The problem was discovered when the producing establishment was notified by their wafer supplier that the chocolate wafers are being recalled because they may contain peanut residue, a known allergen, which is not declared on the label. The Canadian Food Inspection Agency (CFIA) notified FSIS that the recalled wafers were used in products distributed to the United States.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers with questions about the public health alert can contact Maple Leaf Foods Inc. at 1‑877‑526‑4520. Members of the media who have questions can contact Maple Leaf Foods Inc. at media.hotline@mapleleaf.com.
WASHINGTON, Jan. 19, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that the gravy component of ready-to-eat Hy-Vee beef pot roast entrée products may contain wheat, a known allergen, which is not declared on the finished product label. FSIS is issuing this public health alert to ensure that consumers with an allergy to wheat are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The beef pot roast entrée products were produced on various dates between December 26, 2022 and January 17, 2023. The following products are subject to the public health alert [view labels]:
11.6 oz. plastic containers containing “HyVee mealtime BEEF POT ROAST DINNER” with Best If Use By dates of 01/03/2023 - 01/24/2023 and lot codes of 22361‑23017.
25.5 oz. plastic containers containing “HyVee mealtime BEEF POT ROAST DINNER” with Best If Used By dates of 01/02/2023 - 01/24/2023 and lot codes of 22360‑23016.
The products bear establishment number “EST. 51558” inside the USDA mark of inspection. These items were shipped to retail locations in Illinois, Iowa, Kansas, Minnesota, Missouri, Nebraska, South Dakota, and Wisconsin.
The problem was discovered when the establishment identified that they received a substitute gravy mix from their spice supplier that includes wheat, whereas the normal gravy mix does not. The establishment notified FSIS that the label on the back of the product does not list wheat contained in the substitute gravy mix.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some products may be in consumers’ refrigerators or freezers. Consumers with a wheat allergy who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Tina Potthoff, Senior Vice President of Communications of Hy-Vee, at 515‑559‑5770 and tpotthoff@hy-vee.com.
WASHINGTON, Jan. 11, 2023 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert because A & S Produce Inc., a Vernon, Calif. establishment conducting business as Greenland Food Company, produced and distributed fully cooked, frozen swai fried fish cutlet products without the benefit of federal inspection. A recall was not requested because the products are no longer available for purchase.
The fully cooked, frozen swai fried fish cutlet products were produced from July 2022 to September 2022 and have a shelf life of two years. The following product is subject to the public health alert [view label]:
1-lb. vacuum-packed packages containing “Fried Fish Cutlet.”
The products involved in this public health alert do not bear the establishment number or a USDA mark of inspection. These items were sold at retail locations in California and through online sales.
FSIS discovered the problem when it was conducting surveillance at an online retailer and found FSIS-regulated products without a USDA mark of inspection.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact Mimi Jang, owner of A & S Produce Inc., at 323‑260‑5100.
WASHINGTON, Dec. 5, 2022 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ground beef sold at La Michoacana Meat Market, in Greenville, Tex., after a sample of the product tested positive for the presence of Escherichia coli (E. coli) O157:H7. A recall was not requested because there is no product currently available for sale to consumers; however, the ground beef product may remain in consumers’ homes and could cause illness if eaten.
The raw ground beef was ground in store on Nov. 28, 2022. The product was packaged for consumers behind the meat counter in varying weights. The following product is subject to the public health alert [view labels]:
Varying weights of ground beef packed in butcher paper, containing “CARNE MOLIDA REGULAR/GROUND BEEF” with “Packed On” dates ranging Nov. 28 to Dec. 1, 2022, and “Sell By Dec. 1 2022” on the label.
These items were only sold in La Michoacana Meat Market retail store, located at 5106 Wesley St., Greenville, Texas, 75402. The last date that the product was available for sale was Dec. 1, 2022.
The problem was discovered during routine FSIS product testing when a sample confirmed positive for the presence of E. coli O157:H7. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
E. coli O157:H7 is a potentially deadly bacterium that can cause dehydration, bloody diarrhea, and abdominal cramps 2–8 days (3–4 days, on average) after exposure the organism. While most people recover within a week, some develop a type of kidney failure called hemolytic uremic syndrome (HUS). This condition can occur among persons of any age but is most common in children under 5-years old and older adults. It is marked by easy bruising, pallor, and decreased urine output. Persons who experience these symptoms should seek emergency medical care immediately.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume ground beef that has been cooked to a temperature of 160 F. The only way to confirm that raw ground beef is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, https://www.fsis.usda.gov/safetempchart.
Media and consumers with questions regarding the public health alert can contact Jacqueline Ramos, Director of Legal Affairs, La Michoacana Meat Market, at 713‑547‑4621.
WASHINGTON, Nov. 30, 2022 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that fully cooked summer sausage products may be contaminated with extraneous materials, specifically plastic. A recall was not requested because the products are no longer available for purchase.
The fully cooked summer sausage products were produced on July 13, 2022. The following products subject to the public health alert are [view labels]:
1-lb. chubs containing “JET HIGH PRAIRIE MEATS SUMMER SAUSAGE” with lot code 220715 represented on the label.
1-lb. chubs containing “FANTASMA’S finest SUMMER SAUSAGE” with lot code 220715 represented on the label.
The products bear establishment number “EST. 31865” inside the USDA mark of inspection. These items were shipped to retail locations in Kansas and Missouri and additional locations through online sales.
The problem was discovered when the firm notified FSIS that they received a customer complaint reporting clear plastic embedded within multiple packages of summer sausage products.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the recall can contact Louis Fantasma, Paradise Locker Meats Plant Manager, at 816‑945‑9278 or louis@paradisemeats.com.
WASHINGTON, October 13, 2022 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that a specific ground beef product may be contaminated with E. coli O103. A recall was not requested because the products are no longer available for purchase.
The raw ground beef items were produced on October 4, 2022. The following product is subject to the public health alert view labels:
1-lb. plastic vacuum-packed packages containing “FRANK’S BUTCHER SHOP GROUND BEEF” with “PACKED ON” dates of 10‑07‑2022 and 10‑09‑2022 on the label.
The establishment’s retail store location in Hudson, Wyoming sold the affected product directly to consumers. FBS Hudson is actively attempting to contact consumers who may have purchased 14 packages of ground beef product subject to the public health alert.
The problem was discovered when FBS Hudson alerted FSIS that its routine microbial testing results found Shiga toxin-producing E. coli (STEC) O103 in a sample of the ground beef. There have been no confirmed reports of illness due to consumption of these products.
Many clinical laboratories do not test for non-O157 STEC, such as O103 because it is harder to identify than STEC O157:H7. People can become ill from STECs 2‑8 days (average of 3‑4 days) after consuming the organism.
Most people infected with STEC O103 develop diarrhea (often bloody) and vomiting. Some illnesses last longer and can be more severe. Infection is usually diagnosed by testing of a stool sample. Vigorous rehydration and other supportive care is the usual treatment; antibiotic treatment is generally not recommended. Most people recover within a week, but, rarely, some develop a more severe infection. Hemolytic uremic syndrome (HUS), a type of kidney failure, is uncommon with STEC O103 infection. HUS can occur in people of any age but is most common in children under 5 years old, older adults and persons with weakened immune systems. It is marked by easy bruising, pallor and decreased urine output. Persons who experience these symptoms should seek emergency medical care immediately.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume ground beef that has been cooked to a temperature of 160°F. The only way to confirm that ground beef is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, https://www.fsis.usda.gov/safetempchart.
Media with questions regarding the public health alert can contact Jared Hamilton, FBS Hudson VP Plant Operations, at 307‑332‑3655 or hudson@franksbutchershop.com. Consumers with questions regarding the public health alert can contact Cortney Mole, FBS Hudson Store Manager, at 307‑332‑2975 or hudson@franksbutchershop.com.
WASHINGTON, Oct. 1, 2022 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert because Family Fare, a Chippewa Falls, Wisc. establishment, produced ready-to-eat chili cheese wieners that may be contaminated with Listeria monocytogenes. A recall was not requested because it is believed that the products are no longer in commerce.
The ready-to-eat chili cheese wieners were produced on Sept. 21, 2022. The following products are subject to the public health alert [view labels]:
15-oz. vacuum-packed packages containing “Our Local SMOKEHOUSE Chili Cheese flavored Wieners” with a use by date of January 19, 2023.
The products bear establishment number “695SEWI” inside the USDA mark of inspection. These items were shipped to a Family Fare retail location in Cannon Falls, Minnesota, where three packages of the wieners were sold.
The problem was discovered when the Wisconsin Department of Agriculture reported to FSIS that some product was found to be contaminated with Listeria monocytogenes during routine testing.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Media and consumers with questions regarding the public health alert can contact press@spartannash.com.
WASHINGTON, Sept. 16, 2022 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that the raw, ready-to-cook chicken entrée products may contain egg, a known allergen, which is not declared on the finished product label. FSIS is issuing this public health alert to ensure that consumers with an allergy to eggs are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The bacon-cheddar chicken entree products were produced on Sept. 9, 2022. The following products are subject to the public health alert [view labels]:
12 oz. plastic wrapped metal containers containing “aprons READY TO COOK MEAL FOR ONE BACON-CHEDDAR SMOTHERED CHICKEN” with a use by date of 9/21/2022.
The products bear establishment number “P-48176” inside the USDA mark of inspection. These items were shipped to Publix locations in Alabama, Florida, Georgia, North Carolina, South Carolina, Tennessee, and Virginia.
The problem was discovered when the establishment notified FSIS that they received notification from their customer that an incorrect label was on the back of the plastic wrapped metal container. The label on the back of the product contains information related to a chicken cordon bleu product, which does not contain egg. The bacon cheddar chicken product contains egg.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some products may be in consumers’ refrigerators or freezers. Consumers with an egg allergy who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Diana Butz, Retail Compliance Manager of Tampa Bay Fisheries, at 813‑752‑8883, extension 208.
WASHINGTON, Sept. 10, 2022 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that ground beef products in HelloFresh meal kits may be associated with Escherichia coli (E. coli) O157:H7 illness. A recall was not requested because the products are no longer available for purchase.
The meal kits containing ground beef for this public health alert were shipped to consumers from July 2‑21, 2022. The following products are subject to the public health alert [view label]:
10-oz. plastic vacuum-packed packages containing “GROUND BEEF 85% LEAN/15% FAT” with codes “EST#46841 L1 22 155” or “EST#46841 L5 22 155” on the side of the packaging.
The ground beef packages bear “EST.46841” inside the USDA mark of inspection and on the plastic ground beef package.
FSIS, the Centers for Disease Control and Prevention, and state public health partners are investigating an outbreak of E. coli O157:H7 and raw ground beef is the probable source of the reported illnesses. Traceback information identified that multiple case-patients received ground beef produced at establishment M46841 and distributed by HelloFresh in meal kits from July 2‑21, 2022. Traceback of materials used to produce the ground beef is ongoing and FSIS continues to work with suppliers and public health partners on the investigation.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away.
FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume ground beef that has been cooked to a temperature of 160 F. The only way to confirm that ground beef is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, https://www.fsis.usda.gov/safetempchart.
Media and consumers with questions regarding the public health alert can contact hello@hellofresh.com or by live chat.
WASHINGTON, August 24, 2022 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for poultry and meat products containing a Food and Drug Administration (FDA) regulated corn starch that has been recalled due to an undeclared allergen, specifically milk. FSIS is issuing this public health alert to ensure that consumers are aware that these products should not be consumed. This situation is currently evolving, which means additional products may be added. Please continue to check back for possible updates.
While this public health alert focuses on chicken and pork tamale products, FSIS believes it is likely that additional meat and poultry products will be affected by the FDA-regulated corn starch. The list of products subject to the public health alert are available here and the labels are available here. The tamales were shipped to warehouse, distributor, and retail locations in Illinois, Indiana, and Wisconsin. However, if other products are added, additional states might be affected.
FSIS and FDA are coordinating on the recalled corn starch and are working together to determine the extent of the distribution of the corn starch to other establishments.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ homes. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
WASHINGTON, August 23, 2022 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for Perdue’s frozen ready-to-eat (RTE) chicken breast tenders “gluten free” that may be contaminated with extraneous materials, specifically small pieces of clear plastic and blue dye. A recall was not requested because the product is no longer available for purchase.
The frozen RTE chicken breast tenders “gluten free” were produced on July 12, 2022. The following product is subject to the public health alert [view labels]:
42 oz. plastic bags containing “PERDUE CHICKEN BREAST TENDERS GLUTEN FREE” with a “Best if Used By: 07 12 23” and a lot number of 2193 above the use by date.
The products bear establishment number “P-33944” immediately below the “Best if Used By:” date on the back of the plastic bag. These items were shipped to BJ's Wholesale Club retail locations nationwide.
The problem was discovered when the establishment reported to FSIS that it received a complaint from a consumer reporting a chicken tender had a small piece of clear plastic and blue dye inside it.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Members of the media with questions about the public health alert can contact Andrea Staub, Senior Vice President of Perdue Foods LLC, at 410‑341‑2755 or by email at andrea.staub@perdue.com. Consumers with questions may call the Perdue Foods LLC hotline at 866‑866‑3703.
WASHINGTON August 18, 2022 - The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that specific ground beef products may be adulterated with E. coli O157:H7. A recall was not requested because the products are no longer available for purchase.
The "Hawaii Big Island Beef" brand ground beef products were produced on August 8, 2022. The following products are subject to the public health alert [view labels]:
1-lb. vacuum sealed packages containing "Ground Beef (80) Fine 1#/pkg" with "Packed 08/08/22" and "Lot 220808" on the label and case code "134R1".
1-lb. vacuum sealed packages containing "Ground Beef (Ln) Fine 1#/pkg" with "Packed 08/08/22" and "Lot 220808" on the label and case code "135R1".
2-lb. vacuum sealed packages containing "Ground Beef (80) Fine 2#/pkg" with "Packed 08/08/22" and "Lot 220808" on the label and case code "134R2".
10-lb. bags containing "Ground Beef (80) Fine 10# Poly Bag" with "Packed 08/08/22" and "Lot 220808" on the label and case code "0134P10".
10-lb. vacuum sealed packages containing "Ground Beef (75) Fine 10# Vac Seal" with "Packed 08/08/22" and "Lot 220808" on the label and case code "130R10".
10-lb. vacuum sealed packages containing "Ground Beef (80) Fine 10# Vac Seal" with "Packed 08/08/22" and "Lot 220808" on the label and case code "134R10".
40-lb. box containing four 10-lb chubs of "Ground Beef (80) Fine 10#" with "Packed 08/08/22" and "Lot 220808" on the label and case code "0134".
The products bear establishment number "EST. 1063" inside the USDA mark of inspection. These items were shipped to retail and restaurant locations in Hawaii.
The problem was discovered by FSIS during an assessment of the establishment’s production records associated with a sample that tested positive for E. coli O157:H7.
There have been no confirmed reports of adverse reactions due to consumption of these products.
Anyone concerned about an illness should contact a healthcare provider. E. coli O157:H7 is a potentially deadly bacterium that can cause dehydration, bloody diarrhea and abdominal cramps 2‑8 days (3‑4 days, on average) after exposure the organism. While most people recover within a week, some develop a type of kidney failure called hemolytic uremic syndrome (HUS). This condition can occur among persons of any age but is most common in children under 5-years old and older adults. It is marked by easy bruising, pallor, and decreased urine output. Persons who experience these symptoms should seek emergency medical care immediately.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume ground beef that has been cooked to a temperature of 160 F. The only way to confirm that ground beef is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, https://www.fsis.usda.gov/safetempchart.
Media and consumers with questions regarding the public health alert can contact Matt Fornoff, General Manager of Hawaii Beef Producers, LLC, at (808) 776‑1109.
WASHINGTON, July 12, 2022 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that the salad dressing component of ready-to-eat (RTE) Caesar salad with chicken may contain egg, a known allergen, which is not declared on the finished product label. FSIS is issuing this public health alert to ensure that consumers with an allergy to eggs are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.
The Caesar salads with chicken were produced on July 5, 2022. The following products are subject to the public health alert [view labels]:
9 oz. plastic clamshell containers of “TRADER JOE’S CAESAR SALAD WITH WHITE CHICKEN MEAT and Creamy Caesar Dressing” with best by dates of 07/11/22 and 07/12/22, and a lot code of GHNW 186‑06.
The products bear establishment number “P-46987” inside the USDA mark of inspection. These items were shipped to Trader Joe’s locations in Idaho, Oregon, and Washington.
The problem was discovered when the producing establishment notified FSIS that they were informed by a store that the salad dressing packets in the Caesar salad product appeared incorrect. The dressing packets with the salad contain Sweet and Spicy Vinaigrette and not the Creamy Caesar Dressing. These dressing packets are unlabeled and contain egg, which is not declared on the finished product packaging.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS has verified the affected products are no longer available for sale but is concerned that some products may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers with questions about the public health alert can contact GH Foods NW, LLC Customer Service at 888‑449‑9388. Members of the media with questions about the public health alert can contact Neila Alamo, GH Foods NW, LLC, at nalamo@calavo.com.
WASHINGTON, July 7, 2022 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for rendered pork fat products that were produced without the benefit of federal inspection. A recall was not requested because the products are no longer available for purchase.
The rendered pork fat items were produced on various dates from Nov. 26, 2021, to April 29, 2022. The following products are subject to the public health alert [view labels]:
1.8-lb. plastic containers of "MANTECA RENDERED PORK FAT DON PANCHITO"
The products bear establishment number "EST. 19900" inside the USDA mark of inspection. These items were shipped to a warehouse distributor in Bronx, New York.
FSIS was notified by the New York State Department of Agriculture and Markets that the rendered pork fat products were produced and shipped into commerce without the benefit of FSIS inspection. These products are misbranded due to the unauthorized use of the marks of federal inspection.
There have been no confirmed reports of illness or adverse reactions due to consumption of these products. Anyone concerned about an illness or reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers' refrigerators or pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the recall can contact Mr. Francisco Flores, President of Don Panchito Deli & Grocery Corp at 212‑828‑9097.
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