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
Teva Pharmaceuticals is recalling 47,890 units of ParaGard T 380A intrauterine contraceptives in New York and Kentucky due to a failed sterility test.
NABI is recalling 39 model year 2012 31LFW city transit buses because the steering column support bracket may not be properly welded, potentially causing steering failure.
Chrysler is recalling 2014 Dodge Durango, Jeep Cherokee, and Grand Cherokee vehicles because the adaptive cruise control system may cause unintended continued acceleration after the driver releases the pedal.
Ameritrail is recalling specific 2011 Ranch King trailers because a defective hydraulic pump component may cause a loss of braking ability, increasing the risk of a crash.
Tactical Vehicle Outfitters is recalling modified 2010-2014 Ford F-350 and F-550 trucks because oil leaks from the PTO pressure switch may ignite the exhaust thermal blanket.
Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Sacha Inchi Seeds because the product contains undeclared milk, a major food allergen.
Jaguar is recalling 2013-2014 XF vehicles because the rear brake pipe may wear and leak fluid, increasing crash risk.
Kia is recalling 2014 Cadenza vehicles with 19-inch non-chrome aluminum wheels because they may fracture from impacts, increasing crash risk.
Ford is recalling all-weather driver-side floor mats for 2006-2011 Ford, Mercury, and Lincoln vehicles because they may shift and interfere with the accelerator pedal.
Trident is recalling Series 2 ultraviolet pool sanitation systems because electrical arcing can cause them to catch fire. Consumers should unplug the units and contact Trident for a free repair kit.
Ford is recalling 2011-2013 Explorers because an intermittent connection in the electric power steering gear can cause a loss of power steering assist, increasing crash risk.
Terex is recalling 2006-2014 TLM series aerial devices installed on Ford F550 vehicles due to a potential frame crack that could cause loss of control.
Sunbeam is recalling about 151,600 Holmes ceramic heaters because they can overheat and pose a fire hazard. Consumers should stop using the units and contact Sunbeam for a refund.
Schindele Enterprises is recalling XZEN Platinum dietary supplements because they contain undeclared sildenafil and tadalafil, which were marketed without FDA approval.
Schindele Enterprises is recalling Boost Ultra sexual enhancement supplements because they contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Fisher & Paykel Healthcare is recalling infant nasal CPAP prongs and starter kits because the prongs may detach from the tubing, interrupting therapy.
Pfizer is recalling specific lots of Effexor XR 150 mg capsules because a foreign Tikosyn capsule was found in a bottle.
Herbal Give Care Llc is recalling Esbelder Fem Mezcla con L-Carnitina because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Herbal Give Care Llc is recalling Esbelin Siloutte Mezcal Herbal because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Tendex is recalling Naturect Capsules because FDA analysis found the product contains undeclared tadalafil, making it an unapproved drug.
Herbal Give Care Llc is recalling Esbelder Man Herbal Blend because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Schindele Enterprises is recalling ExtenZe 600 mg tablets because they contain undeclared sildenafil or tadalafil, which were marketed without an approved NDA or ANDA.
Herbal Give Care Llc is recalling Esbelin Siloutte Te herbal tea because it contains undeclared sibutramine and related compounds, making it an unapproved new drug.
Human Science Foundation is recalling PRO ArthMax tablets because FDA analysis found unapproved prescription drugs in the product.
Ben Venue Laboratories is recalling 5,131 vials of Acetylcysteine Solution, USP, 10% due to the presence of glass particulate matter.