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
Anderson Compounding Pharmacy is recalling 58 vials of Prostaglandin Tri-Mix 20:30:1 due to a lack of sterility assurance. The recall covers all lots distributed nationwide.
Anderson Compounding Pharmacy is recalling HCG 11,000 mcg Injection vials nationwide due to a lack of sterility assurance.
MSM Nutraceuticals is recalling Red Eye Eye Drops because the product lacks assurance of sterility and was not tested per USP 71.
Anderson Compounding Pharmacy is recalling Lidocaine 1%/Dextrose 12.5% Injection vials due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Gentamicin irrigation syringes due to a lack of sterility assurance. The recall covers all lots distributed nationwide.
Anderson Compounding Pharmacy is recalling Phenylephrine 1 mg/mL Injection vials nationwide because the product lacks sterility assurance.
Anderson Compounding Pharmacy is recalling 22 vials of Sermorelin 0.3 mg/0.5 mL nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Prostaglandin Tri-Mix Injection due to lack of sterility assurance. The recall covers all lots distributed nationwide.
ICU Medical is recalling specific lots of ChemoClave Vial Spikes because they may contain plastic burr particulate from the protective cap used during assembly.
Anderson Compounding Pharmacy is recalling Heparin and Lidocaine syringes due to a lack of sterility assurance. The recall covers all lots distributed nationwide.
Anderson Compounding Pharmacy is recalling Prostaglandin Tri-Mix 60:30:1 Injection due to a lack of sterility assurance. The recall covers all lots distributed nationwide.
Anderson Compounding Pharmacy is recalling 99 vials of HCG 20 Day Extra Strength nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Methylcobalamin 1 mg/mL Injection vials due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Vitamin D3 200,000 IU/mL Injection vials nationwide due to a lack of sterility assurance.
Toyota is recalling 2015-2017 Yaris vehicles because wire harnesses for side air bag sensors may crack and corrode, potentially causing air bags to fail to deploy or deploy improperly.
Toyota is recalling 2019 Sienna vehicles because incorrect welds in the passenger front door may affect air bag sensor readings, potentially causing unintended deployment or failure to deploy.
Forest River is recalling 2019 Rockwood and Flagstaff recreational trailers because improperly installed air conditioning wiring may contact a heat strip, increasing the risk of fire.
Honda is recalling 2017-2018 Clarity Fuel Cell vehicles because internal corrosion may cause the water pump to fail, potentially leading to a vehicle stall and increased crash risk.
Arctic Cat is recalling about 9,000 snowmobiles because the exhaust can flame from the muffler outlet, posing a fire hazard.
Mercedes-Benz is recalling 2019 A 220 and A 220 4MATIC vehicles because improper welding may cause the pedal plate to bend, impairing brake pedal operation and increasing crash risk.
Bendix is recalling ADB22X Air Disc Brake Calipers for school buses because the driver side rear brakes may drag, increasing the risk of fire.
Tekno Products is recalling Tuff smoke-less grills because they can overheat, posing fire and burn hazards. Consumers should stop using the grills and return them for a refund.
General Motors is recalling 2017-2019 Chevrolet Trax vehicles because improperly welded front lower-control arm joints may break, causing partial separation and increased crash risk.
USA LESS Inc. is recalling Leopard Miracle Honey because it contains undeclared sildenafil, an unapproved drug for erectile dysfunction.
Health Solutions Pharmacy Center is recalling compounded Papaverine-Phentolamine-PGE1 injectables because FDA inspectors observed insanitary conditions during the compounding of sterile drugs.