BIMBO Bakeries USA Sunbeam 12 Enriched Hamburger Buns and Sunbeam 12 recall — FDA F-1567-2013
Due to the possible presence of metal fragments caused by a faulty manufacturing part at a North Carolina bakery
Track recent U.S. food recall enforcement reports from the FDA. Review recalled products, reasons, classifications, recalling firms, distribution details and official record identifiers when available.
19,449 detailed records are currently available in this category.
Due to the possible presence of metal fragments caused by a faulty manufacturing part at a North Carolina bakery
Raw material supplier of the chocolate used for the bar coating had milk ingredients added inadvertently. One report of ampholytic reaction.
Raw material supplier of the chocolate used for the bar coating had milk ingredients added inadvertently. One report of ampholytic reaction.
Products with the specific Lot Code and UPC Codes listed above are being retrieved because there is the potential that some of the bottles could exhibit spoilage or damage to the lip of the…
Products with the specific Lot Code and UPC Codes listed above are being retrieved because there is the potential that some of the bottles could exhibit spoilage or damage to the lip of the…
The product has the potential to contain polysaccharide-based bacterial biofilm, mold, and red water mites.
Products with the specific Lot Code and UPC Codes listed above are being retrieved because there is the potential that some of the bottles could exhibit spoilage or damage to the lip of the…
Raw material supplier of the chocolate used for the bar coating had milk ingredients added inadvertently. One report of ampholytic reaction.
The product packaging for Lighthouse Farmer's Market Veggie Burgers may contain Lightlife Kick'n Black Bean Burgers which contain milk. The milk allergen is not declared on the Farmer's…
The firm initiated this recall of "American Ginseng" because FDA lab analysis found pesticide residues.
Products with the specific Lot Code and UPC Codes listed above are being retrieved because there is the potential that some of the bottles could exhibit spoilage or damage to the lip of the…
Products with the specific Lot Code and UPC Codes listed above are being retrieved because there is the potential that some of the bottles could exhibit spoilage or damage to the lip of the…
Raw material supplier of the chocolate used for the bar coating had milk ingredients added inadvertently. One report of ampholytic reaction.
Oskri Corp. of Lake Mills, WI is recalling 1650 (5 pack) of "Sesame Bars Date Syrup" because they may contain copper shavings.
Raw material supplier of the chocolate used for the bar coating had milk ingredients added inadvertently. One report of ampholytic reaction.
Undeclared allergen, soy flour, due to repacking error.
The product is being recalled because it was manufactured using pistachios recalled by Setton Pistachios of Terra Bella, CA because it has the potential to be contaminated with Salmonella.
Blessing Seafood, Inc. is voluntarily recalling one lot of Blessing Inc. Wild White EZ Peel Shrimp due to undeclared sulfites.
The firm was notified by the Ohio Department of Agriculture that several of their labels are missing the the allergin declaration contains wheat.
The firm recalled the Thai chili peppers because FDA analytical results revealed the presence of Salmonella.
The firm was notified by the Ohio Department of Agriculture that several of their labels are missing the the allergin declaration contains wheat.
The firm was notified by the Ohio Department of Agriculture that several of their labels are missing the the allergin declaration contains wheat.
The firm was notified by the Ohio Department of Agriculture that several of their labels are missing the the allergin declaration contains wheat.
The firm was notified by the Ohio Department of Agriculture that several of their labels are missing the the allergin declaration contains wheat.
FDA enforcement reports are classified by potential health hazard. Class I is the most serious classification, while Class II and Class III generally indicate lower levels of risk. The classification shown here comes from the official FDA record.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.