Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Danisco USA Inc. is recalling Grindsted CFF 1455 Stabilizer System due to potential Salmonella contamination. The product was distributed to commercial customers in 24 US states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Sweetlife CINN. Roll BAS Stabilizer & Emulsifier System due to potential Salmonella contamination. The product was distributed across 28 U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Germantown Stabilizer 1772-II, a food stabilizer and emulsifier system, due to potential Salmonella contamination. The product was distributed across the U.S., Canada, and Mexico.
Hormel Foods is recalling PLANTERS Honey Roasted Peanuts 4oz packages due to possible Listeria monocytogenes contamination. Approximately 15,132 packages were distributed to retailers in FL, GA, AL, NC, and SC.
Danisco USA Inc. is recalling Germantown Dari Whip II, a food stabilizer and emulsifier product, due to potential Salmonella contamination. The product was distributed across 23 US states, Canada, and Mexico.
Hormel Foods is recalling Planters Deluxe Lightly Salted Mixed Nuts (8.75 oz) due to possible Listeria monocytogenes contamination. The recall affects 6,804 cans distributed to five southeastern states.
Danisco USA Inc. is recalling Grindsted SSD 6018 Stabilizer System due to potential Salmonella contamination. The product has been distributed to customers in the United States, Canada, and Mexico.
Honda is recalling certain 2013-2023 Honda Accord, Civic, CR-V, HR-V, Odyssey, Pilot, Ridgeline and Acura ILX, MDX, RDX, RLX, TLX vehicles because the fuel pump inside the fuel tank may fail, potentially causing engine stall while driving and increasing crash risk.
Atrium Medical is recalling FLIXENE vascular grafts due to complaints of separation between the Swivel Rod and Swivel Core components. The recall affects 53,308 units worldwide, including 11,236 in the US.
Atrium Medical recalls ADVANTA VXT vascular grafts due to reports of swivel rod separation from the swivel core. Affected units distributed worldwide; healthcare providers should evaluate appropriate management.
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reports of the swivel rod separating from the swivel core. Patients and healthcare providers should contact the manufacturer for guidance.
Atrium Medical Corporation is recalling ADVANTA VXT vascular graft devices due to reports of the swivel rod separating from the core. The separation could compromise device function.
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts because the Slider GDS Swivel Rod may separate from the Swivel Core. A total of 53,308 units are affected.
FDA recalls Atrium Medical's FLIXENE vascular grafts due to reports of the swivel rod separating from the core, potentially compromising device integrity.
Becton Dickinson is recalling 2,061 kits of BD SARS-CoV-2 Reagents for BD MAX Systems because they may produce false negative results due to decreased enzyme activity. The kits were distributed nationwide and internationally.
Atrium Medical recalls ADVANTA VXT vascular grafts due to separation of the slider swivel rod from its core. The defect affects 53,308 units distributed worldwide.
Schreiber Foods is recalling Ranch Garlic Cream Cheese Spread due to potential Salmonella contamination. Approximately 835,721 units were distributed to 19 states and Puerto Rico.
Della Fattoria, LLC is recalling Della Fattoria Sicilian Semolina bread due to missing sesame seed declarations on the label. Consumers with sesame allergies should not consume this product.
Atrium Medical is recalling ADVANTA VXT vascular grafts due to separation of the slider mechanism. The defect affects over 53,000 units distributed worldwide and could compromise graft function.
Atrium Medical is recalling ADVANTA VXT vascular grafts due to reports of the slider rod separating from the swivel core, which could impair proper device function.
Atrium Medical recalls FLIXENE vascular grafts due to complaints of slider rod separation from the swivel core, which could affect device function.
Charles Boggini Company is recalling Cola Flavoring Base due to undeclared sulfites. The product may trigger allergic reactions in sulfite-sensitive individuals.
Once Upon a Farm Organic Plant-Rich Meal (Curried Carrots & Beans) is being recalled due to potential Listeria monocytogenes contamination. The frozen meal is distributed across nine states and has a best-by date of 4/17/2025.
Atrium Medical's ADVANTA VXT vascular grafts are being recalled worldwide due to reports of the Slider GDS Swivel Rod separating from the Swivel Core. The separation creates a gap that could compromise device function.
A defective drip chamber in the Alaris Pump Infusion Set may detach from the tubing, potentially delaying treatment or causing unintended exposure to medications. BD is recalling approximately 11,300 units distributed across the US and Canada.