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
Roush is recalling 2015 Ford Mustang GT Roush Stage 3 vehicles because a brake caliper guide pin may loosen, reducing rear braking ability and increasing crash risk.
Polaris is recalling about 4,700 model year 2015 snowmobiles because the steering pitman arm or drag link can crack, causing a loss of steering and posing a crash hazard.
Polaris is recalling about 2,230 RZR XP Turbo recreational off-highway vehicles because an oil drain line leak can cause a fire.
General Motors is recalling 2016 Chevrolet Silverado and GMC Sierra trucks because a misplaced mounting stud may cause the air bag sensor housing to fracture, potentially preventing air bag deployment in a crash.
Mr Goodcents Inc is recalling Fresh Baked Giant Cookies due to potential peanut contamination. The product was distributed to six states.
Life Science Pharmacy Inc. is recalling E3 Cream compounded in Harriman, NY, due to potential penicillin cross-contamination.
Geritrex Corp is recalling GRx HiCort 25 suppositories because the FDA determined they are unapproved new drugs and misbranded.
Western Drug is recalling two containers of Butor/Nal/Hydro Nasal Suspension because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling Toradol 60mg/mL Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling all lots of Jessners Dermal Solution because the product lacks assurance of sterility. The recall covers distribution in eight US states.
Western Drug is recalling Dep-Estradiol 10 mg/mL Injection because the company cannot ensure the product is sterile. The recall covers 9 containers distributed nationwide.
Western Drug is recalling Squaric Acid 4% Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling all lots of Quad Mix Strong Injections because the company cannot ensure the product is sterile. The recall covers distribution in eight US states.
Western Drug is recalling Furosemide 20 mg/mL solution because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling Hydroxocobalamin 1mg Injections because the company cannot guarantee the product is sterile.
Western Drug is recalling 16 containers of Triamcin40/Lido5 mg/mL Sus due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Philips Medical Systems is recalling 16 Allura Xper cardio systems because the monitor ceiling suspension system may fall.
Western Drug is recalling Folic Acid Injection due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Western Drug is recalling 9 containers of PZI 40 Insulin (Human) because the product lacks assurance of sterility.
Western Drug is recalling 18 containers of Omnitrope 17.4U/10mL Injection Kits due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Chrysler is recalling 2015-2016 Jeep Cherokees with power liftgates because water leaks into the control module, creating a fire risk.
Western Drug is recalling 68 containers of Tri-Mix ED Injection because the product lacks assurance of sterility. The recall covers distribution in eight U.S. states.
Life Science Pharmacy Inc. is recalling Methyfolate Capsules due to potential penicillin cross contamination. The recall is nationwide and affects all lots.
Life Science Pharmacy Inc. is recalling Methyfolate Injection due to potential penicillin cross-contamination. The recall covers all lots distributed nationwide.
Life Science Pharmacy Inc. is recalling compounded Estriol Vaginal Gels due to potential penicillin cross-contamination. The recall covers all lots distributed nationwide.