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
Pharmacy Creations is recalling EDTA disodium 150 mg/mL sterile injection vials due to a lack of assurance of sterility.
Beacon Hill Medical Pharmacy is recalling Triple-Testosterone oil injection solutions because FDA inspections raised concerns about quality control and sterility assurance.
Beacon Hill Medical Pharmacy is recalling DMSO 50% Injectable due to FDA inspectional findings regarding quality control and sterility assurance.
The FDA is recalling Monoject flush syringes that may contain non-sterile water instead of saline or heparin, posing a risk of infection.
Beacon Hill Medical Pharmacy is recalling Alprostadil injection due to FDA inspectional findings regarding quality control and sterility assurance.
Beacon Hill Medical Pharmacy is recalling Selenium 400 mcg/mL injectable because FDA inspections raised concerns about quality control and sterility assurance.
Beacon Hill Medical Pharmacy is recalling Ascorbic Acid 500 mg/mL injectable due to FDA inspectional findings regarding sterility assurance.
Wellness Pharmacy is recalling RL Glutathione 100 mg/mL vials due to laboratory results indicating microbial contamination and concerns about the reliability of testing.
Beacon Hill Medical Pharmacy is recalling Pyridoxine HCL Injectable due to FDA inspectional findings regarding quality control and sterility assurance.
Beacon Hill Medical Pharmacy is recalling Testosterone Propionate 100 mg/mL oil injection solution because FDA inspections raised concerns about sterility assurance and quality control.
Waterlogic is recalling about 48,000 chiller-based water dispensers because the hot water tank can stop functioning and cause the machine to overheat, posing a fire hazard.
Pierce is recalling 2012-2013 Velocity and Arrow XT emergency vehicles because a valve defect may prevent parking brakes from engaging, increasing crash risk.
Newmar is recalling 2012 Essex and King Aire motor homes because air pressure gauges may be inaccurate, potentially hiding low air brake pressure and increasing crash risk.
Vactor is recalling 2012-2013 Ramjet vehicles with Allison Transmissions because incorrect software may allow the vehicle to enter drive mode while the power take-off is in use.
Gree is recalling 12 brands of dehumidifiers due to fire and burn hazards. Consumers should unplug the units and contact Gree for a refund.
Mitsubishi Fuso is recalling 2013-2014 FEC52, FEC72, FEC92, and FGB72 trucks because transmission oil cooler hoses may leak fluid, potentially causing the transmission to fail and increasing crash risk.
Terex is recalling 1997-2013 XT55 and XT60 aerial devices because cracks in the boom hinge may cause the platform to fall, risking injury.
Beamonstar Products is recalling SexVoltz All Natural Herbal Supplement because it contains tadalafil, an unapproved drug ingredient.
Zip International Group LLC is recalling Baltic Sprats in Spicy Brine because the product may be contaminated with Listeria monocytogenes.
Beamonstar Products is recalling Velextra All-Natural Herbal Supplement because it contains tadalafil, an unapproved drug ingredient.
Conagra is recalling Kroger Break 'N Bake Chocolate Chip Cookie Dough because peanut butter was present but not listed on the label.
Saratoga Therapeutics is recalling ebA Multivitamin tablets because they contain milk components despite labeling stating they are free of milk.
Dove Chocolate Discoveries is recalling 18 oz boxes of Fruit Collection Dark Chocolate due to mislabeling. The boxes contain Cinnamon Dusted Dark Chocolate Almonds instead of the labeled fruit mix.
Terrafina is recalling specific varieties of salted pistachios due to potential Salmonella contamination. The products were distributed in New York, New Jersey, and Florida.
Terrafina is recalling five varieties of unsalted pistachios due to potential Salmonella contamination. The products were distributed in New York, New Jersey, and Florida.