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
Kids II is recalling all Rocking Sleepers because five infant deaths have occurred. Consumers should stop using the product and contact the company for a refund.
Mitsubishi is recalling 26,016 2017-2018 Mirage G4 vehicles because a software error may disable air bags. Dealers will reprogram the system free of charge.
Fenton Mobility is recalling 2015-2018 Ford Transit vehicles equipped with specific foldaway seats that may fail to lock in place during a crash, increasing injury risk.
FCA US is recalling 2018-2019 Ram 1500 trucks because an incomplete weld on the rear driveshaft may crack or fracture, creating a road hazard or loss of drive power.
General Motors is recalling specific 2017-2019 Chevrolet Silverado and GMC Sierra trucks because a short circuit in the engine block heater could cause a fire.
Mazda is recalling 2011-2013 Mazda6 vehicles sold or registered in specific states because the front cross member may corrode, potentially affecting steering alignment.
Volvo is recalling 2019 S60 vehicles because rear suspension lock nuts may not be properly tightened, which could cause sudden handling changes and increase crash risk.
Little Red Rooster Company is recalling NadaMoo! Strawberry Cheesecake Non-Dairy Frozen-Dessert because it contains undeclared almonds.
The FDA is recalling Kopi Jantan Tradisional Natural Herbs Coffee because it contains undeclared sildenafil and tadalafil, unapproved drugs for erectile dysfunction.
Anderson Compounding Pharmacy is recalling Serum Tears 50% Ophthalmic Drops due to a lack of sterility assurance. All lots are affected nationwide.
Anderson Compounding Pharmacy is recalling Prostaglandin Tri-Mix 30:30:1 Injection vials nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Methylcobalamin 3000 mcg/mL Injection Solution due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Neomycin 40 mg/Polymixin B 200,000 Bladder Irrigation Solution due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Prostaglandin Tri-Mix 50:30:1 vials nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling 23 vials of Prostaglandin 20 mcg/mL due to a lack of sterility assurance. The product was distributed nationwide.
Anderson Compounding Pharmacy is recalling HCG 20 Day Injection vials nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Testosterone Cypionate 250 mg/mL sterile injections because the product lacks sterility assurance.
Brainlab AG is recalling Spine & Trauma 3D Navigation 1.0 software because it may display fixed image planes instead of the desired inline view, potentially preventing surgeons from determining instrument position.
Anderson Compounding Pharmacy is recalling specific 60 mL syringes containing Heparin, Marcain, Sodium Bicarbonate, and Normal Saline due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling 12 syringes of a Heparin, Marcain, and Sodium Bicarbonate mixture due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Heparin and Marcaine syringes due to a lack of sterility assurance. The recall covers all lots distributed nationwide.
Anderson Compounding Pharmacy is recalling Prostaglandin Quad-Mix Injection vials due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling HCG 23 Day vials nationwide due to a lack of sterility assurance. Consumers should stop using the product.
Anderson Compounding Pharmacy is recalling HCG 40 Day Injection Extra Strength vials nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Atropine 0.01% Eye Drops because the product lacks sterility assurance. The recall covers all lots distributed nationwide.