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Updated: March 29, 2023 7:12 PM
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The FDA is currently investigating an outbreak of Salmonella Infantis. As of March 29, 2023, a total of 12 people infected with Salmonella Infantis have been reported. No specific product has been linked to this investigation as of today. This investigation is ongoing.
Salmonella is an organism... See More that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis, and arthritis.
In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Source: fda.gov See Less
Salento Organics of West Palm Beach, Florida is recalling its 4 ounce packages of Dark Chocolate Pitaya Bites, Dark Chocolate Goldenberry Bites, Dark Chocolate Mango Bites, Dark Chocolate Banana Bites, Dark Chocolate Pineapple Bites and Dark Chocolate Peanut Bites because they may contain undeclared milk. People who... See More have allergies to milk run the risk of serious or life-threatening allergic reaction if they consume these products. These products were distributed nationwide in retail stores and through mail orders. No illnesses have been reported to date in connection with these products.
The list of recalled products is shown in the image below.
Consumers who have purchased the affected products are urged to return them to the place of purchase for a full refund.
In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: Salento Organics
Brand name: Salento Organics
Product recalled: Various Dark Chocolate Fruit and Peanut Bites
Reason of the recall: Undeclared Milk
FDA Recall date: March 29, 2023
Source: fda.gov See Less
Gilster Mary Lee, 10 Industrial Park, Steeleville Illinois is recalling one lot of HyVee Hamburger Chili Macaroni Skillet Meal, UPC 75450-08552 at the consumer level because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of a serious... See More life- threating allergic reaction if they consume this product. The recalled product was sold at HyVee Retail Stores and Dollar Fresh Market Stores in Iowa, Illinois, Missouri, Kansas, Nebraska, South Dakota, Minnesota and Wisconsin. No illnesses have been reported to date in connection with this product.
The only lot involved is HyVee Hamburger Chili Macaroni Skillet Meal, packaged in 5.2-oz. cartons which have a Best By date of FEB 08 24 Y18 (UPC# 75450-08552). Consumers should return the product to the store for a full refund or discard it.
Gilster-Mary Lee Corp. became aware of the mispackaging after receiving an email from a customer.
In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: Gilster-Mary Lee Corp.
Brand name: HyVee
Product recalled: Hamburger Chili Macaroni Skillet Meal
Reason of the recall: Undeclared Milk Allergen
FDA Recall date: March 29, 2023
Source: fda.gov See Less
North American Food Distributing Company, Inc of West Sacramento, Ca is recalling 16.9 fl oz of Kagome Worcester Sauce and 16.9 fl oz of Kagome Chuno Sauce, because it may contain undeclared soy. People who have an allergy or severe sensitivity to Soy or Soy products run... See More the risk of serious or lifethreatening allergic reaction if they consume these products. At this moment, No illnesses have been reported to date. Distributed in Northern California through retail grocery stores throughout the area.
The products are identified as:
-Brand: Kagome, Type: The Worchester Sauce, Size: 16.9 fl oz plastic bottle, UPC code: 4901306097502
-Brand: Kagome, Type: The Chuno Sauce, Size: 16.9 fl oz plastic bottle, UPC code: 4901306097519
In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: North American Food Distributing Company, Inc.
Brand name: Kagome
Product recalled: Worcester Sauce; Chuno Sauce
Reason of the recall: Undeclared Soy
FDA Recall date: March 29, 2023
Source: fda.gov See Less
The FSIS announced the recall of approximately 3,436 pounds of boneless beef chuck product by Elkhorn Valley Packing because it may be contaminated with Shiga toxin-producing E. coli (STEC) O103. This product was shipped to distributors, federal establishments, retail locations, and wholesale locations, which includes hotels, restaurants,... See More and institutions, in Connecticut, Illinois, Indiana, Maryland, Massachusetts, Michigan, New Jersey, New York and Pennsylvania. There have been no confirmed reports of adverse reactions due to the consumption of this product.
The recalled product is:
- Various weights corrugated boxes containing “Elkhorn Valley Pride Angus Beef 61226 BEEF CHUCK 2PC BNLS; Packed on 2/16/23.” The complete list of serial numbers and box count numbers for the boneless beef chuck product that are subject to recall can be found in the image below.
The product subject to recall was packed on Feb. 16, 2023 and bears the Establishment number “EST. M-19549” inside the USDA mark of inspection.
The recall was initiated when FSIS testing of ground beef derived from the product revealed a positive result for STEC O103. STEC O103 can cause diarrhea (often bloody) and vomiting, typically appearing 2-8 days (average of 3-4 days) after consumption. 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 but can occur in people of any age, particularly young children, older adults, and those with weakened immune systems.
Consumers are advised not to use or further distribute the product, and to throw it away or return it to the place of purchase. To ensure the product is cooked to a temperature high enough to kill harmful bacteria, a food thermometer should be used to measure the internal temperature.
In case you are experiencing E. coli symptoms such as watery diarrhea (often bloody), vomiting; stomach cramps; and mild fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Source: fsis.usda.gov See Less
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anonymous17323
What distributors processed this meat? What retailers sold it to consumers? I have been sick for 5 days. No updates from any govt agencies or health departments. I'll probably get my stool sample results back before the govt/media tell us where the beef was sold. Filed report with USDA FSIS and they forwarded to my state department of health. Still waiting for someone to tell me if I was poisoned at my grocery deli counter
The FSIS announced the recall of approximately 1,455 pounds of smoked baby rope sausage by Kelley Foods due to misbranding and an undeclared allergen. The product contains cheese, thereby milk, a known allergen, which is not declared on the product label. This product was shipped to retail... See More locations in Alabama and Florida. There have been no confirmed reports of adverse reactions due to the consumption of this product.
The recalled product is:
- 12-oz. vacuum-packed packages containing “KELLEY Naturally Hardwood Smoked JALAPEÑO PEPPER BABY ROPE SAUSAGE” code 2705493011 and a use or freeze by date of May 11, 2023.
The recalled product was produced on Jan. 10, 2023 and bears the establishment number “EST. 8016” inside the USDA mark of inspection.
The problem was discovered when the firm notified FSIS that a grocery store manager found that the Kelley Foods Jalapeño Pepper Baby Rope Sausage appeared to contain cheddar cheese, which was not listed as an ingredient on the product label. Upon further investigation, the firm confirmed that its jalapeño and cheddar baby rope sausage product contained the wrong label.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. If you have an allergy or are sensitive to milk do not eat it, it may cause a serious or life-threatening reaction. Please throw it away or return it to the place of purchase.
In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Source: fsis.usda.gov See Less
FDA announced the recall of 231,071 cases (2,772,852 cans) of Kirkland Signature Colombian Cold Brew Coffee ready-to-drink by Berner Foods Inc. due to the presence of foreign material (metal). This product was distributed in Georgia, New Jersey, California, Maryland, Michigan, Illinois, Washington, Arizona, Utah, Florida, Colorado, Texas... See More and Minnesota.
The recalled product is:
- Kirkland Signature Colombian Cold Brew Coffee ready-to-drink, 12 fl oz in aluminum can, 12 cans per case. Codes: Lot#231019 Best If Used By: 10 19 23; Lot#231020 Best If Used By: 10 20 23; Lot#231021 Best If Used By: 10 21 23; Lot#231022 Best If Used By: 10 22 23; Lot#231023 Best If Used By: 10 23 23; Lot#231024 Best If Used By; 10 24 23; Lot#231025 Best If Used By: 10 25 23; Lot#231026 Best If Used By: 10 26 23; Lot#231027 Best If Used By: 10 27 23.
If you have the recalled product in your home, please do not eat it, throw it away.
In case you experienced harm from extraneous materials, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.
Source: accessdata.fda.gov See Less
Second Nature Brands of Madison Heights, MI, is recalling its 4-ounce packages of Gluten Free Reese’s Pieces Brownie Brittle because they may contain undeclared wheat. The recalled Gluten Free Reese’s Pieces Brownie Brittle were distributed nationwide in retail stores and through online orders. One illness has been... See More reported to date in connection with this problem, to date.
People who have an allergy or severe sensitivity to wheat run the risk of serious or life-threatening allergic reaction if they consume these products.
The product comes in a 4-ounce pouch UPC 711747011562 marked with lot codes SG 1054 15/NOV/2023 1S and SG 1054 15/NOV/2023 2S on the backside of pouch.
The recall was initiated after it was discovered that the gluten-containing product was distributed in packaging that did not reveal the presence of wheat. Subsequent investigation indicates the problem was caused by cross-contamination at a co-manufacturer, resulting in undeclared wheat in the product.
Production of the product has been suspended until FDA and the company are certain that the problem has been corrected.
Consumers who have purchased 4-ounce packages of Gluten Free Reese’s Pieces Brownie Brittle with lot codes SG 1054 15/NOV/2023 1S and SG 1054 15/NOV/2023 2S should not consume the product and should contact Brownie Brittle for a full refund.
In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: Second Nature Brands
Brand name: Sheila G’s
Product recalled: Gluten Free Reese’s Pieces Brownie Brittle
Reason of the recall: Undeclared Wheat
FDA Recall date: March 23, 2023
Source: fda.gov See Less
Perfection Bakeries D/B/A Aunt Millie’s of Fort Wayne, IN. is recalling 8 ct. packages of Our Family® White Hot Dog Buns because they may contain undeclared sesame. People who have an allergy or severe sensitivity to sesame run the risk of serious or life- threatening allergic reaction... See More if they consume these products. The recalled product was distributed in retail stores in Michigan, Ohio, Indiana, and Illinois. 1 reaction has been reported to date in connection with this recall.
The product comes in a printed plastic package marked with “Our Family Hot Dog Buns 8 ct.” on the top and has a blue twist tie. The product UPC is 0-70253-75107-3, and include Best By Dates 4-9-2023 and earlier.
The recall was initiated after it was discovered the sesame-containing product was distributed in packaging that did not reveal the presence of sesame. Production of the product has been suspended until the FDA and Aunt Millie’s complete their investigation and are certain the market has been cleared of any incorrect packaging.
Consumers who have purchased "Our Family Hot Dog Buns 8 ct." are urged to return them to the place of purchase for a full refund.
In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: Perfection Bakeries D/B/A Aunt Millie’s
Brand name: Our Family
Product recalled: White Hot Dog Enriched Buns
Reason of the recall: Potential or Undeclared Allergen/Sesame
FDA Recall date: March 22, 2023
Source: fda.gov See Less
Seven Seas International USA, LLC of St. Petersburg, Florida is voluntarily recalling 295 cases of Biltmore Smoked Sockeye Salmon because Listeria monocytogenes may be present in some product. This product was sold by Publix and Publix GreenWise Market.
The recalled product is:
- Biltmore Smoked Sockeye Salmon,... See More GTIN: 73621188774, Lot/Exp date: R4058
The issue was discovered through routine regulatory testing conducted by the Florida Department of Agriculture and Consumer Services.
Consumers who have purchased the recalled product are being advised not to consume it and return it to the store where it was originally purchased for a full refund.
In case you are experiencing Listeria monocytogenes symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Source: corporate.publix.com See Less
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