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
Pfizer Inc. is recalling 102,500 vials of Vancomycin Hydrochloride for Injection due to the presence of glass particulate matter.
The FDA is recalling Natural Herbal Coffee AMPT because it contains undeclared sildenafil, tadalafil, and milk. The product was marketed without an approved NDA or ANDA.
Old Dutch Foods is recalling Cheddar & Sour Cream flavored potato chips because a seasoning ingredient may contain milk contaminated with Salmonella.
Thor Motor Coach is recalling 2018 Freedom Traveler motorhomes because a missing heat shield between the propane tank and generator exhaust pipe increases the risk of fire.
Aldi is voluntarily recalling Choceur Dark Chocolate Bars because they may contain undeclared almond pieces, a tree nut allergen.
Advanced Pharma Inc. is recalling 550 syringes of NitroGlycerin injection found to be subpotent. The product was distributed nationwide to hospitals and medical facilities.
Amneal Pharmaceuticals is recalling Lorazepam Oral Concentrate because dropper measurement markings may be reversed, shifted, or missing, which could lead to dosing errors.
Vital Rx, Inc. is recalling all sterile products due to poor aseptic production practices identified during an FDA inspection.
Advanced Pharma Inc. is recalling 320 syringes of Nitroglycerin injection that were found to be subpotent, meaning they contain less active ingredient than labeled.
L. Perrigo Company is recalling Zephrex-D nasal decongestant softgels due to microbial contamination. Consumers should stop using the product and return it to the pharmacy.
Creative Contract Packaging is recalling HERB-OX Beef Flavor Granulated Bouillon due to potential undeclared milk allergen.
Swift Beef Company is recalling approximately 4,702 pounds of beef stew products sold in Texas due to possible contamination with plastic and metal.
Newmar is recalling 2017 Bay Star, Bay Star Sport, and Canyon Star motorhomes because missing plugs in the brake system may cause fluid leaks or air ingestion, increasing stopping distance.
MV Agusta is recalling 2015-2017 F4 RC and F4 RR motorcycles because the front brake master cylinder may fail, increasing crash risk.
PFP Enterprises LLC is recalling approximately 7,570 pounds of ground beef products due to misbranding and an undeclared soy allergen. The raw, frozen products were shipped to distributors and institutions in Texas.
Hyundai Translead is recalling 2017 Composite and HyCube trailers because improperly torqued brake caliper bolts may allow the caliper to detach, increasing crash risk.
Melville Direct is recalling Bits and Pieces Fiber Optic Christmas Trees because the AC power adapter can overheat, posing a fire hazard.
Forest River is recalling 2015-2018 Cherokee and Cascade recreational trailers because improperly routed wiring may be pinched, creating a fire hazard.
Polaris is recalling about 560 RZR XP 4 Turbo vehicles because an improperly secured fuel line can leak and cause a fire.
Forest River is recalling 2018 Prime Time Crusader and Sanibel trailers because a missing furnace bracket may allow carbon monoxide leaks or fire.
Maserati is recalling 2018 Quattroporte and Ghibli vehicles because a fuel delivery pipe may leak, increasing the risk of a fire.
Walker is recalling 2018 Tank Trailers because improperly torqued brake caliper bolts may allow the caliper to detach, causing a loss of braking ability.
Wabash National is recalling 2018 Truck Body vehicles because a missing weld on the vertical leg support increases injury risk in rear-end collisions.
FCA US LLC is recalling 2018 Alfa Romeo Giulia and Stelvio vehicles because contaminated brake fluid may damage the braking system and reduce performance.
Sun Pharmaceutical Industries is recalling Riomet (metformin hydrochloride) oral solution due to microbial contamination. The recall covers specific lots of the cherry-flavored prescription liquid.