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
Northwest Compounding Pharmacy is recalling specific lots of compounded Cyclosporin liquid 2% for dry eye due to a lack of sterility assurance. The product was distributed in Oregon.
Northwest Compounding Pharmacy is recalling HCG liquid vials because they may lack sterility assurance. The product was distributed in Oregon to medical facilities and patients.
Northwest Compounding Pharmacy is recalling MIC B vitamin liquid due to a lack of sterility assurance. The product was distributed in Oregon to medical facilities and patients.
Northwest Compounding Pharmacy is recalling Testosteron Cypionate liquid 200mg/ml because of a lack of sterility assurance. The product was distributed in Oregon to medical facilities, a physician's office, and patients.
Northwest Compounding Pharmacy is recalling compounded Cyclosporin liquid 0.2% due to a lack of sterility assurance. The product was distributed in Oregon to medical facilities and patients.
Northwest Compounding Pharmacy is recalling Vitamin B12 liquid 1000mcg/ml due to lack of sterility assurance. The product was distributed in Oregon to medical facilities and patients.
Northwest Compounding Pharmacy is recalling Epinephrine liquid 1:1000 in 50 ml glass vials due to a lack of sterility assurance. The product was distributed in Oregon to medical facilities and patients.
Northwest Compounding Pharmacy is recalling Lidocaine/Epinephrine liquid 1%/1:1000 in 50 ml glass vials due to a lack of sterility assurance. The product was distributed in Oregon to medical facilities and patients.
Toyota is recalling approximately 1.3 million vehicles because front passenger air bag inflators may explode due to humidity, potentially causing serious injury or death.
Subaru is recalling specific 2010-2014 models because passenger air bag inflators may explode during deployment, potentially causing serious injury or death.
Northwest Compounding Pharmacy is recalling Cyclosporin liquid 0.05% due to a lack of sterility assurance. The product was distributed in Oregon to medical facilities and patients.
Northwest Compounding Pharmacy is recalling compounded Cyclosporin liquid 0.5% in plastic dropper bottles due to a lack of sterility assurance. The product was distributed in Oregon to medical facilities, a physician's office, and patients.
J. H. Routh Packing Co. is recalling approximately 1,719 pounds of raw pork sausage products that may contain rubber. The products were shipped to retail locations in Kentucky, Ohio, and Pennsylvania.
Northwest Compounding Pharmacy is recalling Lidocaine gel 2% due to a lack of sterility assurance. The product was distributed in Oregon to medical facilities and patients.
Subaru is recalling specific 2010-2014 models because front passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Ferrari is recalling various models from 2014 to 2018 because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Daimler Vans USA is recalling 2014-2017 Freightliner and Mercedes-Benz Sprinter vans because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Daimler Vans USA is recalling 2015-2017 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because driver air bag inflators may explode during deployment.
Motor Coach Industries is recalling specific 1997-2015 coaches because a steering defect may cause loss of control at highway speeds.
Keystone RV is recalling 2017-2019 Dutchmen Voltage and 2019 Endurance travel trailers because tires may contact the rear floor support, affecting handling.
Ford is recalling specific 2010-2014 models because passenger air bag inflators may explode due to humidity, posing a serious injury risk.
Tesla is recalling 2014-2016 Model S vehicles because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Vantage Mobility International is recalling 2014-2017 AMS Edge II vehicles because a deteriorating fuel pump gasket may cause fuel leaks, increasing fire risk.
Advanced Pharma Inc. is recalling 225 syringes of Phenylephrine HCl injectable solution because the label incorrectly states the concentration as 10 mcg per mL instead of 100 mcg per mL.
Takata is recalling certain frontal passenger air bag inflators in 2011 and newer vehicles registered in 22 states and D.C. due to a risk of explosion.