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.
18,152 detailed records are currently available in this category.
IQF 1/4" White Onion Dice is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Product manufactured with roasted sunflower kernels which may be contaminated with Listeria monocytogenes.
Haiati Matdongsan Peanut Crunch Snack, 80g and 325g, plastic flex bag is being recalled because it contains Soy Lecithin and this was not listed on the finished product labeling.
3/8" Frozen Yellow Onion Dice was voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Possible contamination with Listeria monocytogenes
IQF 1/4" Frozen Yellow Onion Dice is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Product manufactured with roasted sunflower kernels which may be contaminated with Listeria monocytogenes.
3/8" White Onion Dice- FRESH is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Procesadora de Frutos y Vegetales del Caribe SRL, Calle Club Rotario 24, Madre Vieja Sur, San Crist¿bal, Dominican Republic has initiated a voluntary recall due to an undeterminable number…
IQF 3/8" Frozen Yellow Onion Strip and IQF 3/8" Yellow ORGANIC Onion Strip are voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Product was found to contain metal fragments.
IQF 3/4" Frozen Yellow Onion Dice is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
IQF 3/8" Un-Blanched, Frozen, Yellow Onion Dice is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Product manufactured with roasted sunflower kernels which may be contaminated with Listeria monocytogenes.
Baptista's Bakery is recalling The Snack Factory 30 oz. Original Pretzel Crisps due to undeclared milk, because it may contain seasoned pretzel crisps which utilize dairy in their topical…
Chili and taco seasoning products contain an ingredient which was recalled for potentially containing undeclared wheat allergen. Testing revealed the presence of gluten. Wheat is not…
Sundae Shoppe Novelty Ice Cream Dipped "Variety" Ice Cream Cones are being recalled because they may contain peanuts which are not declared on the allergen statement.
A sample of raw cucumbers tested positive for Salmonella spp.
Foreign matter (plastic) was observed in the product.
Chili and taco seasoning products contain an ingredient which was recalled for potentially containing undeclared wheat allergen. Testing revealed the presence of gluten. Wheat is not…
The firm was notified by their supplier that the Sunflower kernels they received may be contaminated with Listeria monocytogenes.
Potential presence of Listeria Monocytogenes
Macaroni Salad with Cheddar Cheese is recalled due to the potential to be contaminated with Listeria monocytogenes. This product contains affected green peas that were recalled by National…
Deli-Food Chili & Spice LLC announces a voluntary field action for Ancho Chile Powder due to positive testing for Salmonella.
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.
