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.
1) The product contained undeclared sulfites (7984 ppm) based on sampling and analysis by New York State Department of Agriculture & Markets. 2) The product contained undeclared sulfites…
Product labeling is incorrect, FD&C colors are undeclared.
Product labeling is incorrect, FD&C colors are undeclared.
Product labeling is incorrect, FD&C colors are undeclared.
Wegmans Foods Markets issued a Press Release on April 16, 2013 and is recalling affected units of Roasted Red Pepper Dip because some of the tubs may have an incorrect ingredient label that…
Products potentially contaminated with E. coli O121.
Product labeling is incorrect, FD&C colors are undeclared.
Product labeling is incorrect, FD&C colors are undeclared.
Product labeling is incorrect, FD&C colors are undeclared.
Product labeling is incorrect, FD&C colors are undeclared.
The firm failed to include allergen milk on the label of this sauce.
The firm failed to include allergens of wheat and anchovy on the label of this marinade. Soy sauce is listed, but soy is not listed as the source of the sauce.
Product labeling is incorrect, FD&C colors are undeclared.
Product labeling is incorrect, FD&C colors are undeclared.
Product labeling is incorrect, FD&C colors are undeclared.
The firm failed to include allergens of milk and soy on the label of this sauce.
Products potentially contaminated with E. coli O121.
The firm failed to include allergens of soy and anchovy on the labels of this sauce.
Product labeling is incorrect, FD&C colors are undeclared.
The firm failed to include allergens of soy and anchovy on the label of this sauce.
Bake House Granola, does not list the source of the unsalted butter ingredient as milk, an allergen. People who have an allergy or severe sensitivity to milk, run the risk of serious or…
Product contains undeclared almonds
Nexgen Pharma is recalling a certain lot of dietary supplement L-Arginine L-Ornithine Alpha Lipoic Acid Capsules due to subpotency of the Alpha Lipoic Acid ingredient.
In response to a FDA inspection, the firm initiated the recall because the product was found to be contaminated with Staphylococcus Aureus, E. Coli, and Alkaline Phosphatase.
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.
