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.
16,964 detailed records are currently available in this category.
The recall was initiated due to New York City Department of Health and Mental Hygiene laboratory results from two samples of Karawan brand tahini testing positive for Salmonella. The recall…
The recall was initiated due to New York City Department of Health and Mental Hygiene laboratory results from two samples of Karawan brand tahini testing positive for Salmonella. The recall…
Suppliers pre harvest field test was returned positive for Salmonella
70% Dark Chocolate Buttons products are recalled due to undeclared soy lecithin.
Product is recalled due to undeclared egg.
Product was labeled as gluten free by mistake, but the product does contain Gluten.
FDA inspection found that allergen sub ingredients are not declared on the label - wheat, soy, milk.
The recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.
The recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.
Products containing almonds and pecans were distributed in packaging that was mislabeled and did not reveal the presence of almonds and pecans.
The product does not provide adequate nutrition for some infants.
FDA inspection found that allergen sub ingredients are not declared on the label - wheat, soy, milk.
Products containing almonds and pecans were distributed in packaging that was mislabeled and did not reveal the presence of almonds and pecans.
Unilever is voluntarily recalling a limited quantity of Ben & Jerry s Coconut Seven Layer Bar bulk and Ben & Jerry s Chunky Monkey pints, because product contains undeclared tree nuts,…
Products containing almonds and pecans were distributed in packaging that was mislabeled and did not reveal the presence of almonds and pecans.
Jalapeno peppers may be contaminated with Salmonella.
FDA inspection found that allergen sub ingredients are not declared on the label - wheat, soy, milk.
Products containing almonds and pecans were distributed in packaging that was mislabeled and did not reveal the presence of almonds and pecans.
The recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.
Unilever is voluntarily recalling a limited quantity of Ben & Jerry s Coconut Seven Layer Bar bulk and Ben & Jerry s Chunky Monkey pints, because product contains undeclared tree nuts,…
One of the firm's direct accounts notified that three out of six samples of Farmed Fresh Atlantic Salmon tested positive for Listeria monocytogens.
Product team in Japan discovered that the product does not declare coconut as an ingredient or allergen.
The recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.
Some chocolate products imported from Japan do not have the English label for Nutrition facts, ingredients or allergens, which include milk, soy, egg, tree nuts.
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.
