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
Country Fresh Inc. is recalling specific pineapple products due to potential contamination with Listeria monocytogenes.
The FDA is recalling Race Trac Melon Trio due to potential Listeria monocytogenes contamination. Consumers should not consume this product until further notice.
Siemens Medical Solutions is recalling Artis zee and Artis Q systems because a software defect may cause the equipment to collide with room fixtures or patients.
Country Fresh Inc. watermelon products are recalled because they may contain Listeria monocytogenes, a harmful bacterium.
Seafarers, Inc. is recalling two lots of frozen yellowfin tuna loins after four people became ill with symptoms including rash and diarrhea.
The FDA is recalling Seasonal Fruit Trays 40oz due to potential Listeria monocytogenes contamination. Consumers should not consume these products until further notice.
Mitsubishi Fuso is recalling 2019-2021 FEC7T, FEC9T, and FECZT trucks because loose exhaust studs may allow hot gases to leak, increasing fire risk.
Heartland is recalling 2019-2020 Milestone fifth-wheel trailers because outriggers may bend from rear storage loading, increasing crash risk.
Taher, Inc. is recalling approximately 22,096 pounds of frozen meat products produced without federal inspection. The products were shipped to institutions and food service locations in Minnesota.
Shyft Group is recalling 2021 Utilimaster Aeromaster vehicles because a body mount bracket may chafe brake lines, potentially reducing braking ability and increasing crash risk.
Daimler Trucks North America is recalling 2018-2019 Freightliner and Western Star trucks because a clutch component may fail, allowing the vehicle to move unexpectedly.
General Motors is recalling 2,781 2020 Buick, Cadillac, Chevrolet, and GMC SUVs because a fuel pump defect may cause the engine to stall without warning.
Prime-Time Specialty Vehicles is recalling 2014-2019 Ram ProMaster Paratransit vehicles because the transmission shifter cable may disconnect, causing unintended movement.
Zero Motorcycles is recalling 2021 SR, S, DSR, DS, FX, and FXS models because the DC-DC converter may shut off, disabling ABS and lights.
Tim Campbell Farm LLC is recalling flat parsley in wooden crates because the product tested positive for Listeria monocytogenes.
AB ULAX is recalling 1500 Flex Heat and Moisture Exchangers because they may disconnect from the respiratory circuit, potentially causing hypoxia or death.
PD-Rx Pharmaceuticals is recalling 20 bottles of Nature-Throid 1 GR tablets due to CGMP deviations and potential sub-potency. The product was distributed in Arizona and Oklahoma.
Biomet is recalling OnPoint Scope Procedure Kits because they were not properly aligned with the gamma sterilization group, resulting in improper sterilization.
Direct Rx is recalling 26 bottles of Ranitidine 300 mg tablets because the product was found to contain the NDMA impurity.
Direct Rx is recalling specific lots of Ranitidine 150 mg tablets because an NDMA impurity was detected. The affected products were distributed in Florida and Georgia.
Roche Diagnostics is recalling BenchMark ULTRA Advanced Staining Systems due to a risk of fluid leaks causing electrical shorts, heat, and fire.
Bombardier is recalling 2020 Can-Am Ryker motorcycles because improperly installed front wheels may separate, increasing crash risk.
Direct Rx is recalling 33 bottles of Losartan Potassium 100 mg tablets found to contain an impurity above acceptable levels.
Roche Diagnostics is recalling the DISCOVERY ULTRA Advanced Staining System due to fluid leaks that can cause electrical shorts, heat, and smoke.
Daimler Vans USA is recalling 2020 Mercedes-Benz Sprinter vans because damaged brake hoses may leak fluid, increasing crash risk.