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
Alfred Louie Inc. is recalling 10-pound packages of mung bean sprouts because FDA environmental samples found Listeria monocytogenes in the facility.
Aston Martin is recalling specific 2012-2014 models because a manufacturing error may cause the throttle pedal arm to break, preventing the driver from maintaining or increasing engine speed.
Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Ball - Shrimp Ball because the label failed to list egg and the fish species.
Go Max Go Foods is recalling Thumbs Up Candy Bars labeled as dairy-free because they contain undeclared milk.
Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Balls because the label failed to list egg and the specific fish species.
Lloyd Inc. of Iowa is recalling 5.7 million Thyro-Tab tablets because stability failures in previous lots make it impossible to verify the quality of the current lots.
Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Balls because the label failed to list egg as an ingredient and did not declare the species of fish.
Triumph is recalling 2012-2013 Trophy and Trophy SE motorcycles because the fuel tank layers may fail to adhere, causing leaks that could lead to engine stalls or fires.
Yakima is recalling Whispbar rack fitting kits for specific vehicles because they do not fit the roofline properly, creating a crash risk.
Green Valley Drugs is recalling Cyanocobalamin 1000 mcg/mL injection because testing revealed positive sterility results.
Cook Medical is recalling Zilver PTX Drug-Eluting Peripheral Stents because the delivery system's inner catheter can fracture or separate after deployment, a defect linked to one reported death.
Performance Plus Marketing is recalling BLUE Diamond Platinum Capsules because they may contain undeclared sildenafil, tadalafil, and analogues, making them unapproved drugs.
Performance Plus Marketing is recalling Mojo Nights Capsules because they may contain undeclared sildenafil, tadalafil, and analogues, making them unapproved drugs.
Evol Nutrition is recalling Mojo Nights for Her capsules because they contain unapproved ingredients used to treat male erectile dysfunction.
Performance Plus Marketing, Inc. is recalling Blue Diamond Pill male sexual enhancement products because they may contain undeclared sildenafil, tadalafil, and analogues.
Cook Medical is recalling Zilver PTX Drug-Eluting Peripheral Stents due to delivery system fractures and tip separations that resulted in one death.
Consumer Concepts is recalling ROCK-IT MAN capsules because FDA analysis found they contain an unapproved sildenafil analogue.
Performance Plus Marketing is recalling Casanova Capsules because they may contain undeclared sildenafil and tadalafil, making them unapproved drugs.
Green Valley Drugs is recalling Methylprednisolone Preservative Free 40 mg/mL injectable suspension because testing revealed positive sterility results.
Green Valley Drugs is recalling 529 vials of Magnesium Sulfate Injection because the pharmacy could not ensure the products were sterile.
Insolroll is recalling about 1,500 solar and rechargeable motor roller shades because the built-in lithium batteries can overheat and cause fires.
Green Valley Drugs is recalling Lipotropic With Vitamins, Carnitine, Chromium and Glutamine Injection because the pharmacy could not ensure the products were sterile.
Green Valley Drugs is recalling Modified Myers Cocktail Injection vials because the pharmacy could not ensure the products were sterile.
Green Valley Drugs is recalling Estradiol Cypionate Injection because the pharmacy could not ensure the products were sterile. The recall covers all strengths and presentations distributed nationwide.
Lisy Corp. is recalling Adobo sin pimienta in 5 oz, 14 oz, and 32 oz sizes because the product contains undeclared soy.