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.
17,742 detailed records are currently available in this category.
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
The firm was notified that the products may be contaminated with Listeria monocytogenes.
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
The firm was notified that the products may be contaminated with Listeria monocytogenes.
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
Ingredients statement declared whey, powdered cheese and cheddar cheese but did not declare milk. In addition, FD&C colors Yellow #5 and Yellow #6 are not declared.
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
Blue Line Distribution is voluntarily recalling certain pre-mix parbake dough mix products due to the possible presence of pieces of plastic pen, which have been found in certain batches of…
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Recall of four varieties of Probiotic drinks due to premature spoilage. Testing has identified Candida lusitaniae as the predominate microorganism as the cause of spoilage.
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
Product may contain undeclared milk.
Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.
Recall of four varieties of Probiotic drinks due to premature spoilage. Testing has identified Candida lusitaniae as the predominate microorganism as the cause of spoilage.
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
Recall of four varieties of Probiotic drinks due to premature spoilage. Testing has identified Candida lusitaniae as the predominate microorganism as the cause of spoilage.
Recall of vegetable trays and cups after notification that they were made with product recalled by Mann Packing for potential Listeria monocytogenes.
CFIA sampled one salad product which resulted in a positive result for Listeria monocytogenes.
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.
