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
Ungar's Food Products is recalling Dr. Praeger's Gluten Free California Veggie Burgers because they contain undeclared soy.
Elekta is recalling MOSAIQ Oncology Information System software due to a defect that sends incorrect field sizes to treatment machines for stereotactic plans using cones.
Hospira is recalling 314,600 bags of 0.9% Sodium Chloride Injection USP due to potential channel leaks that may compromise sterility.
Vitamin Cottage is recalling Natural Grocers Caribbean Fruit & Nut Mix because macadamia nuts in the product may be contaminated with Salmonella.
ViewRay is recalling three units of Patient Handling System software due to a report of the couch moving unexpectedly into the bore after a reboot.
Owen Mumford USA is recalling Autopen Classic Automatic insulin delivery pens because the dose dial fails to stay set, preventing patients from administering their medication.
Lion Pavilion Ltd. is recalling Grassplot Ginger Slices because the product contains undeclared sulfites. Consumers with this product should stop using it.
Sunrise Global Marketing is recalling GreenWorks 12-amp electric blower/vacs because the motor can catch fire, posing fire and burn hazards.
Fresenius Kabi is recalling 7,593 vials of Rifampin for Injection because the product failed impurity and degradation specifications.
PACCAR is recalling 2016 Kenworth trucks because reversed air brake lines may prevent the redundant braking system from working correctly during a failure.
Acorn Stairlifts is recalling about 34,500 motorized stair lifts because the seat post can separate from the main support, posing a fall hazard.
Nissan is recalling 2015 Sentra, Versa Note, and Rogue vehicles because driver-side doors may not fully latch, posing a crash and ejection risk.
Allied Recreation Group is recalling 92 model year 2016 motorhomes because an incorrect propane regulator may allow moisture buildup, potentially causing a gas leak and fire.
Discount Tire is recalling specific Pathfinder SAT light truck tires because an inner liner gauge defect may cause tread separation and rapid air pressure loss.
Target is recalling about 143,000 Circo Night Lights because the battery can overheat and cause the light to melt, posing a fire hazard.
Mazda is recalling 2007-2014 CX-9 vehicles because front suspension ball joints may corrode, potentially causing loss of steering control and increasing crash risk.
SAF-Holland is recalling CBX series trailer suspension systems because pivot bolts may fail, potentially causing the axle to separate from the trailer and increasing crash risk.
BMW is recalling 2014-2015 MINI Cooper, Cooper S, and John Cooper Works vehicles because rear seats fail federal side impact safety standards, increasing injury risk.
Redwood Hill Farm is recalling one lot of Raw Milk Feta because it tested positive for Listeria monocytogenes.
Bethel Nutritional Consulting is recalling SLIM-K capsules because FDA testing found unapproved ingredients including sibutramine and phenolphthalein.
Murry's, Inc. is recalling approximately 20,232 pounds of Bell & Evans gluten-free breaded chicken nuggets due to staphylococcal enterotoxin contamination.
FDA recalls Shiley tracheostomy tubes due to reports of patient discomfort and breathing difficulties.
Baxter Healthcare is recalling 202,824 bags of 0.9% Sodium Chloride Injection due to the presence of metal particulate matter.
Baxter Healthcare is recalling 402,284 bags of 5% Dextrose Injection due to the presence of metal particulate matter.
United Salad Company is recalling Champ's Sliced Crimini Mushrooms due to potential Listeria monocytogenes contamination. The product was distributed in Oregon and Washington.