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
PACCAR is recalling specific Peterbilt auto haulers because front tires have a lower speed rating than the vehicle's maximum speed, increasing crash risk.
BMW is recalling 2014-2015 MINI Cooper and Cooper S vehicles because incorrectly calibrated seat sensors may cause inappropriate airbag activation or deactivation during a crash.
Cloverdale Foods is recalling beef and pork bratwurst mislabeled as beef frankfurters because it contains undeclared milk, a known allergen.
Boulder Natural Meats is recalling approximately 3,607 pounds of beef, pork, and poultry products due to misbranding and undeclared milk allergen.
Maple Leaf Foods is recalling approximately 4,030 pounds of boneless pork shoulders that entered the U.S. without inspection. The products were shipped to retail locations in California.
Outdoors RV is recalling 2015-2016 Timber Ridge, Glacier Peak, Wind River, and Black Stone trailers because liquid propane hoses and electrical wires may be pinched or scraped, increasing the risk of fire.
Nissan is recalling specific 2015 Altima and 2016 Maxima vehicles because front brake caliper mounting bolts may not be properly tightened, which could reduce braking ability.
Fresca Foods is recalling Sea Salt Crunchy Bean Snacks because ranch-flavored product containing undeclared milk was packaged in sea salt bags.
MCF Operating LLC is recalling Hellmann's Zesty Italian Dressing because it was manufactured with romano cheese that tested positive for Listeria monocytogenes.
JD & SN Inc. is recalling 5 syringes of Testosterone Propionate Injectable Solution due to a lack of assurance of sterility.
JD & SN Inc. is recalling Estradiol 18 mg pellets because the company cannot assure the sterility of the product. The recall covers all sterile human compounded drugs within their expiry date.
The FDA is recalling 9 vials of Chorionic Gonadotropin Injectable Solution from Moses Lake Professional Pharmacy due to a lack of assurance of sterility.
The FDA is recalling Estradiol pellets from JD & SN Inc. because the manufacturer cannot ensure the sterile compounded drugs are free of contamination.
Park Compounding Pharmacy is recalling specific vials of Caffeine + Sodium Benzoate 500mg/mL due to a lack of assurance of sterility.
JD & SN Inc. is recalling 6 syringes of Dexpantenol Injectable Solution because the FDA identified a lack of assurance of sterility.
JD & SN Inc. is recalling TRIMIX injectable solution because the agency could not ensure the product remained sterile. Patients should stop using the medication and contact their healthcare provider.
JD & SN Inc. is recalling 95 vials of Chorionic Gonadotropin because the FDA could not verify the sterility of the compounded drug.
Moses Lake Professional Pharmacy is recalling Estradiol Pellets because the FDA determined there is a lack of assurance of sterility for the compounded drug.
JD & SN Inc. is recalling 298 units of compounded testosterone pellets because the FDA cannot ensure the product is sterile.
The FDA is recalling 36 syringes of Methylcobalamin Injectable Solution because the manufacturer cannot ensure the product is sterile.
JD & SN Inc. is recalling a compounded injectable solution because the FDA could not ensure the product remained sterile. Patients should stop using the medication and contact their healthcare provider.
Park Compounding Pharmacy is recalling specific vials of Methylcobalamin 1000mcg/mL due to a lack of assurance of sterility.
Moses Lake Professional Pharmacy is recalling 355 testosterone pellets because the FDA cannot assure they are sterile. Patients should stop using the product and consult a healthcare provider.
JD & SN Inc. is recalling 8 syringes of Vitamin D3 Oil Injectable Solution due to a lack of assurance of sterility.
FDA is recalling a compounded injectable solution due to a lack of assurance of sterility. The product is distributed nationwide.