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
Federal Coach is recalling 2010 Spirit and Premier buses because voltage spikes may damage door actuator circuit boards, increasing the risk of fire.
Nissan is recalling 2014 Pathfinder, Rogue, and Infiniti QX60 vehicles because a right-side lug nut may not be properly tightened, posing a wheel separation risk.
Coach and Equipment is recalling 2013 Metro Lite and Phoenix buses because a wheelchair lift cable may cause a short circuit and fire.
Polaris is recalling specific 2014-2015 Victory motorcycles because an engine defect may cause the engine to seize, increasing the risk of a crash.
Frontier Natural Products Co-op is recalling various brands of organic whole black peppercorns because testing revealed the presence of Salmonella.
Shire Human Genetic Therapies is recalling 8,359 vials of VPRIV (velaglucerase alfa) because they contain stainless steel and barium sulfate particles.
Dolphin Intertrade Corporation is recalling XIYOUJI QINGZHI CAPSULES because they contain undeclared sibutramine, a substance removed from the U.S. market for safety reasons.
Fossil Fuel Products, LLC is recalling RezzRX capsules because they contain undeclared hydroxylthiohomosildenafil and aminotadalafil.
Dolphin Intertrade Corporation is recalling JaDera weight loss capsules because they contain undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Creative Snacks Co. is recalling dried apricots in cups and bags because they contain undeclared sulfites. The products were distributed in Massachusetts and New Jersey.
Sprouts Farmers Market is recalling Organic Whole Black Peppercorns because FDA tests found Salmonella in one lot and another lot poses a contamination risk.
Lisy Corp. is recalling Sweet Basil Albahaca because an FDA sample tested positive for Salmonella. The product was distributed in four states.
HeartWare Inc is recalling HVAD Pump Implant Kits because the driveline connector housing may separate. This defect could affect patients using the device for heart failure.
General Motors is recalling 1,131,113 vehicles due to a transmission shift cable that may fracture, causing unintended movement or rollaway.
UCI-FRAM is recalling specific ignition switches used in GM vehicles because they may shift out of the run position, causing the engine to stall and disabling air bags.
RaySearch Laboratories is recalling Ray Station software versions 2.0 through 4.0 due to dose miscalculations for support structures on CT images.
Ion Beam Applications is recalling Proteus 235 Proton Therapy System Legacy Software due to incorrect dose rate calculations for non-zero beam line options.
Natural Grocers by Vitamin Cottage is recalling Organic Black Peppercorns due to potential Salmonella contamination.
GE Healthcare is recalling 1,546 MRI scanners worldwide because gradient coil connections may loosen, causing overheating, smoke, and potential fire.
American Pop Corn Co is recalling Jolly Time Microwave Popcorn due to potential contamination with stainless steel metal fragments.
Baxter Healthcare is recalling Sigma Spectrum Volumetric Infusion Pumps due to repeated System Error 322 occurrences.
Brookfield Prescription Center Inc. is recalling one lot of Glycopyrrolate solution for injection due to Bacillus thuringiensis contamination.
Hospira is recalling 255,900 vials of Potassium Chloride for Injection due to the presence of red and black particulate matter identified as iron oxide.
White-Rodgers is recalling about 740,000 digital thermostats in the U.S. and 403,000 in Canada because leaking batteries can cause a fire. Consumers should check for a battery icon on the screen to see if their unit is affected.
IKEA is recalling approximately 3.5 million children's wall-mounted lamps in the U.S. because the electrical cords pose a strangulation risk to infants.