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.
16,072 detailed records are currently available in this category.
Consumer complaints reported presence of white pieces of plastic in cookie product.
During an internal inspection the firm discovered that several products may contain soy lecithin which is not declared on the labels.
Glass pieces found in lot of chocolate covered peanuts.
undeclared non-wheat gluten, product labeled gluten-free
Undeclared allergen; fish (anchovy)
Undeclared allergen; fish (anchovy)
culling not performed to remove rotted apples, excessive levels of patulin found in 1 lot
Physical appearance of bottle of G-Pre Protein was atypical. Once opened, unusual odor was noticed and atypical bubbles were present.
Frozen Tuna may contain elevated levels of Histamine
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Kenover Marketing, 72 New Hook, Bayonne NJ, 07002, has initiated a recall of Mighty Sesame 10.9 Oz Organic Tahini (Squeezable), Squeezable Plastic Jar, 8 Units per Case, UPC: 858313006208…
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
High bacterial growth within products
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
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.
