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 the agency’s own highest classification or reported deaths or serious injuries, 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
Wells Pharmacy Network LLC is recalling 984 vials of MIC/B-Complex Injectable because the product lacks assurance of sterility.
Tri-Coast Pharmacy is recalling TriMix compounded injections because the agency could not ensure the products were sterile.
Tri-Coast Pharmacy is recalling 99 vials of compounded Methylcobalamin/Folic Acid/Pyridoxine injections due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling 5,277 kits of compounded Chorionic Gonadotropin injectable kits nationwide due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling 41 syringes of Mitomycin Solution Injectable because the agency could not ensure the product was sterile.
Wells Pharmacy is recalling 330 Sermorelin Acetate 28 mg Injectable Kits nationwide due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling Tri 1 (PAP/PHEN/ATROPINE) NR Injectable vials because the product lacks assurance of sterility.
Wells Pharmacy Network LLC is recalling 550 vials of Tri-Test 200 Injectable because there is a lack of assurance of sterility. The product was distributed nationwide.
Wells Pharmacy Network LLC is recalling QUAD4 injectable vials because the FDA determined there is a lack of assurance of sterility.
Tri-Coast Pharmacy is recalling 59 vials of Amino Energy Cocktail because the agency cannot assure the sterility of the compounded product.
Tri-Coast Pharmacy is recalling 236 vials of Lipotropic with MIC compounded between May and November 2016 due to a lack of assurance of sterility.
Wells Pharmacy Network LLC is recalling 22 vials of a compounded injectable drug due to a lack of assurance of sterility.
Tri-Coast Pharmacy is recalling 35 vials of TriMix compounded injections because the agency cannot assure the products are sterile.
Hale And Hearty Soups, LLC is recalling White Bean, Broccoli S.D.T. soup due to potential contamination with Listeria monocytogenes.
BMW is recalling 2007-2012 X5 and X6 vehicles because the front passenger air bag inflators may rupture during a crash, potentially causing serious injury or death.
Honda is recalling 2006-2009 and 2012 GL1800 motorcycles because air bag inflators may rupture in a crash, potentially causing serious injury or death.
Honda is recalling specific Acura and Honda models because front passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.
Subaru is recalling 2005-2008 models and 2006 Saab 9-2X vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Mercedes-Benz is recalling specific 2008-2012 models because front passenger air bag inflators may rupture during deployment, potentially sending metal fragments into the vehicle.
Tesla is recalling 2012 Model S vehicles because the front passenger air bag inflator may rupture in a crash, potentially causing serious injury or death.
Jaguar Land Rover is recalling 2007-2012 Range Rovers because front passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Subaru is recalling specific 2005-2012 models because front passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Mitsubishi is recalling 2012 and 2014 i-MiEV vehicles because front passenger air bag inflators may rupture during a crash, potentially causing serious injury or death.
Honda is recalling specific 2006-2012 models because the front passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.
Perfect Fit Meals is recalling approximately 3,546 pounds of chicken breast product because it contains undeclared milk and wheat allergens.