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
General Motors is recalling 2010-2014 Chevrolet Camaros because the ignition key may be accidentally knocked out of the run position by the driver's knee, potentially disabling airbags and power steering.
Honda is recalling specific 2003-2006 vehicles sold or registered in California due to a Takata air bag inflator defect that could rupture during deployment.
Bellisio Foods is recalling Thai Kitchen Chicken Pad Thai frozen entrées because the packaging fails to list soy protein isolate, a known allergen.
General Motors is recalling 2013-2014 Cadillac ATS and 2014 CTS vehicles because the transmission shift cable may detach, causing unintended movement or rollaway.
Altec is recalling 258 aerial trucks because front torsion bar welds could fail, potentially causing vehicle instability and injury to the operator.
General Motors is recalling 2015 Chevrolet Silverado HD and GMC Sierra HD trucks because a power steering hose clamp may disconnect, potentially causing loss of steering and brake assist.
MyNicNaxs, Inc. is recalling REDUCE WEIGHT FRUTA PLANTA Capsules because they contain undeclared phenolphthalein and were marketed without FDA approval.
MyNicNaxs, Inc. is recalling Slim Xtreme Weight loss capsules because they contain undeclared active pharmaceutical ingredients, including sibutramine, and were marketed without FDA approval.
MyNicNaxs, Inc. is recalling Magic Slim capsules because they contain undeclared active pharmaceutical ingredients and were marketed without an approved NDA or ANDA.
MyNicNaxs, Inc. is recalling Fruta BIO 400 mg capsules because they contain undeclared sibutramine and phenolphthalein.
MyNicKnaxs is recalling weight reduction pills marketed without FDA approval because they contain undeclared phenolphthalein.
Pure Edge Nutrition is recalling Bella Vi INSANE AMP'D dietary supplements because they contain undeclared sibutramine and phenolphthalein.
MyNicNaxs, Inc. is recalling Meizi Evolution Soft Gel Capsules because the product was marketed without an approved NDA/ANDA and contains undeclared active pharmaceutical ingredients.
MyNicNaxs, Inc. is recalling Jianfeijindan Activity Girl Capsules because they contain an undeclared sibutramine analog and were marketed without FDA approval.
Pure Edge Nutrition is recalling Bella Vi AMP'D UP weight loss capsules because they contain undeclared sibutramine and phenolphthalein.
Pure Edge Nutrition is recalling Bella Vi BTrim MAX dietary supplements because they contain undeclared sibutramine and phenolphthalein and were marketed without FDA approval.
MyNicNaxs, Inc. is recalling Meizitang Strong Version Botanical Slimming capsules because they contain undeclared active pharmaceutical ingredients, including sibutramine.
Pharmakon Pharmaceuticals is recalling specific lots of Midazolam syringes because they contain twice the stated amount of the drug.
Greenstone LLC is recalling 16,018 bottles of Venlafaxine HCl Extended-Release Capsules because a foreign capsule was found in a bottle from the same packaging campaign.
Pure Edge Nutrition is recalling Bella Vi eXtreme ACCELERATOR capsules because they contain undeclared sibutramine and phenolphthalein.
MyNicNaxs, Inc. is recalling SlimEasy Herbs Capsules because they contain undeclared sibutramine and N-desmethylsibutramine and were marketed without an approved NDA/ANDA.
Vitality Research Labs is recalling vitaliKOR capsules because FDA sampling found undeclared vardenafil and tadalafil. The product was marketed without an approved NDA or ANDA.
Pure Edge Nutrition is recalling Bella Vi BTrim Ultimate Boost capsules because they contain undeclared sibutramine and phenolphthalein.
Pure Edge Nutrition is recalling Bella Vi INSANE Bee Pollen capsules because they contain undeclared sibutramine and phenolphthalein.
MyNicNaxs, Inc. is recalling Super Fat Burning Bomb Capsules because they contain undeclared active pharmaceutical ingredients, phenolphthalein and N-desmethylsibutramine.