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
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges due to compromised sterility caused by a barrier breach.
Baptist Health Medical Towers Pharmacy is recalling Ceftriaxone IV bags in Arkansas due to a lack of sterility assurance.
Thor Motor Coach is recalling 2015-2016 Tuscany motor homes because steering boxes may wear prematurely, risking sudden loss of steering.
Lakota is recalling 2016 Bighorn, Charger, and Livestock Edition trailers because pin holes in aluminum rims may cause tire failure and increase crash risk.
Meritor is recalling specific FF967 Non-Drive Front Steer axles manufactured in 2012 because they may have been incorrectly heat treated, posing a risk of fracture and loss of vehicle control.
Volkswagen is recalling specific 2016 Jetta, Passat, and Golf vehicles because the fuel rail may detach, causing a fuel leak that could lead to a vehicle fire.
Solomon Snacks and Bakery is recalling approximately 873 pounds of meat pies produced without federal inspection and containing undeclared eggs, milk, and wheat.
Butterfield Foods is recalling broccoli salad kits in Indiana and Ohio due to possible Listeria contamination from sunflower kernels.
Hillsdale Furniture is recalling about 20,000 children's bunk beds sold at Bob's Discount Furniture because support rails can crack or break, posing a fall hazard.
West-Mark is recalling 2014-2015 Sugar Tank trailers because improperly seated brake diaphragms may cause drag, potentially leading to wheel end fires.
Tiffin is recalling 2014-2016 Allegro motorhomes because incorrect steering box spacers can cause premature wear, leading to a sudden loss of steering ability and increased crash risk.
Autocar is recalling 18 Xpeditor trucks due to a defective engine control module that may cause the engine to stall unexpectedly, increasing crash risk.
Square Grove is recalling about 750 Sit-Stand Desk Converters because the pneumatic lifting mechanism can pinch or break fingers during assembly or use.
The Sausage Maker, Inc. is recalling Dried Sausage Sticks seasoning because the Fermento ingredient contains undeclared whey protein and skim milk powder.
Master Herbs is recalling Licorice Coughing Liquid because it contains undeclared morphine and was marketed without an approved NDA or ANDA.
R Thomas Marketing, LLC is recalling Weekend Prince capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Baxter Healthcare is recalling 273,520 bags of 0.9% Sodium Chloride Injection USP due to the presence of cardboard particulate matter.
R Thomas Marketing, LLC is recalling Hard Ten Days capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
R Thomas Marketing, LLC is recalling Tiger King capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Super Herbs 350 mg capsules are being recalled because they contain undeclared sibutramine, desmethylsibutramine, and/or phenolphthalein.
R Thomas Marketing, LLC is recalling Samurai-X capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
The FDA is recalling 'Bigger Longer More Time More Sperms' because it was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Pharmakon Pharmaceuticals is recalling 75 syringes of Morphine Sulfate 0.5 mg/mL due to out-of-specification potency results indicating high levels.
Lipo Escultura capsules are being recalled because they contain sibutramine and diclofenac, making them unapproved drugs rather than dietary supplements.
R Thomas Marketing, LLC is recalling Stree Overlord capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).