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
Dairy Fresh LLC is recalling IGA Brand Vanilla & Chocolate Ice Cream because it contains undeclared almonds, coconut, and soy lecithin.
Chrysler is recalling 1993-1998 Jeep Grand Cherokee and 2002-2007 Jeep Liberty vehicles because fuel tanks may leak in rear impacts, posing a fire risk.
Hazelnut Growers of Oregon is recalling bulk in-shell hazelnuts due to potential Salmonella contamination. The product was distributed in Canada.
Southwest Ice Cream Specialties is recalling 1,524 cartons of ice cream because the product may contain undeclared pecan, soy, and/or wheat allergens.
Trophy Nut Co Inc is recalling 6 oz. natural pistachios because they were made with pistachios that may be contaminated with Salmonella.
Kolcraft is recalling Jeep Liberty strollers because tire inner tubes can rupture, causing wheel rims to fly off as projectiles. The defect has resulted in 18 reported injuries.
Pure Herbs, Ltd. is recalling Natural Herbal Extracts Protein Dietary Supplement bottles because they contain undeclared milk and soy allergens, posing a risk of serious allergic reactions.
Ohlins is recalling steering dampers for BMW motorcycles because an incorrectly machined bracket may crack, potentially causing steering to lock and leading to injury or a crash.
Endologix Inc. is voluntarily recalling 53 units of the AFX Introducer System due to reports of dilator breakage during clinical procedures.
Forest River is recalling 289 model year 2014 Sunseeker, Forester, Lexington, and Solera motorhomes because a battery isolation manager short circuit could cause smoke or fire.
Tesla is recalling 1,228 2013 Model S vehicles because a weakened weld on the left second-row seat back may cause it to detach in a crash, increasing injury risk.
North American Bus Industries is recalling 2003-2013 45CLFW and 2013 40CLFW transit buses because the air brake pedal mounting may become loose, increasing crash risk.
General Motors is recalling approximately 193,652 vehicles from 2005-2007 due to a driver's door module defect that could cause a fire.
Temsa is recalling 256 motorcoaches because over-tightened seat belt bolts may fail in a crash, increasing injury risk.
Texsport is recalling about 325 Cedar Lake Propane Heater/Cookers because a malfunctioning regulator can cause propane to flare, posing a fire hazard.
Honda is recalling specific 2006-2007 S2000 and 2006 Acura RSX vehicles because the brake booster may lose vacuum, reducing braking assistance and increasing crash risk.
Whole Foods Market Group Inc. is recalling 493 lbs of Salad Chicken Curry due to an undeclared egg allergen. The product was sold in six northeastern states.
Symbios Medical Products is voluntarily recalling GoPump and GoBlock kits manufactured before July 2012 because they may deliver excessively high flow rates.
Symbios Medical Products is voluntarily recalling GoPump kits because some units may deliver excessively high flow rates.
TG United, Inc. is recalling 386 bottles of TG 40PSE/400GFN tablets because they are underdosed or have an incorrect dosage regime.
Pentec Health is recalling Baxter LL bag 1% Amino Acids because sterility could not be assured for the compounded sterile renal nutritional prescriptions.
TG United, Inc. is recalling ED A-Hist Tablets because they are underdosed or have an incorrect dosage regime.
Symbios Medical Products is voluntarily recalling GoPump Rapid Recovery System kits because some units may deliver medication at excessively high flow rates.
TG United, Inc. is recalling 22,721 bottles of Brompheniramine/Pseudoephedrine DM liquid because the product is underdosed or has an incorrect dosage regime.
Pentec Health is recalling specific lots of IDPN dialysate solution bags because sterility could not be assured. The products were distributed to dialysis centers and directly to patients.