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. has recalled Grindsted SSD 6242 Stabilizer System due to potential Salmonella contamination. The recall affects 884.52 kg of product distributed to the United States, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted IcePro 2427 TH Stabilizer System due to potential Salmonella contamination. The product was distributed across 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.
Danisco USA Inc. is recalling Grindsted WCS 1265 Stabilizer and Emulsifier System due to potential Salmonella contamination. The product was distributed across the US, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted TH GSD 2272 Stabilizer and Emulsifier System distributed in bulk due to potential Salmonella contamination. The product was distributed across the U.S., Canada, and Mexico.
Getinge's sevoflurane vaporizer component may degrade into hydrogen fluoride, posing inhalation and skin exposure risks to healthcare workers and patients. The FDA Class I recall affects 120 units distributed across six U.S. states.
Danisco USA Inc. is recalling GSD 0911 Stabilizer due to potential Salmonella contamination. The food ingredient additive was distributed to manufacturers across the US, Canada, and Mexico.
Danisco USA Inc. is recalling CRE-90 (RO1) Stabilizer System due to potential Salmonella contamination. The product was distributed across multiple US states, Canada, and Mexico.
Danisco USA Inc. is recalling Germantown Enhance Plus Stabilizer System (lot 1204572178) due to potential Salmonella contamination. The product was distributed across multiple US states, Canada, and Mexico.
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.
Danisco USA Inc. is recalling Grindsted SSD 5731 Non-GMO Stabilizer System due to potential Salmonella contamination. The product was distributed across multiple U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Iced Coffee 6880 Stabilizer System because of potential Salmonella contamination. The affected product (lot 1204625920) was distributed in the US, Canada, and Mexico.
Danisco USA Inc. is recalling Yogurt 6626 Stabilizer System due to potential Salmonella contamination. The product was distributed across 23 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.
Multiple brands of yogurt pretzels are being recalled due to potential Salmonella contamination. Affected products were distributed in California and Washington.
The FDA recalled 3,138 Arrow Ultra 8 intra-aortic balloon catheter kits globally due to potential balloon inflation failure and helium pathway damage that could compromise critical cardiac support.
Danisco USA Inc. is recalling Germantown Gard Preservative (25 kg bags) due to potential Salmonella contamination. The product was distributed across the US, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Sweet Roll Dough Blend 2 Stabilizer & Emulsifier System due to potential Salmonella contamination. The product was distributed across the US, Canada, and Mexico.
Danisco USA Inc. recalls Grindsted Sour Cream 6563 stabilizer system for potential Salmonella contamination affecting 33,600 kg distributed across the US, Canada, and Mexico.
Arrow International is recalling its UltraFlex Intra-Aortic Balloon Catheter Kit because of infrequent device malfunction that could lead to serious health consequences. 44,807 units are affected worldwide.
The ADVANTA VXT vascular graft is being recalled because its slider rod can separate from the swivel core, creating a gap between components. No injuries have been reported.
Schreiber Foods Inc is recalling whipped cream cheese spread sold under multiple store brands due to potential Salmonella contamination. Consumers should return the product to the retailer.
Philips is recalling the HA FlexTrak patient transport trolley due to potential oil leaks from the hydraulic system that create slipping and falling hazards. Approximately 100 units have been distributed worldwide.
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.
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the slider rod from its core component. This mechanical failure could compromise device functionality.