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
Honda is recalling specific Acura, Honda, and Isuzu vehicles because driver air bag inflators may rupture or underinflate, posing a risk of injury.
Honda is recalling specific 2000-2003 Acura and Honda vehicles because replacement driver air bag inflators may rupture or underinflate in a crash, increasing injury risk.
Multiquip is recalling 119 2019 WT5C trailers because incorrect safety chain attachment points may interfere with steering and increase crash risk.
BMW is recalling 2000-2006 3-Series and M3 vehicles because front passenger airbag inflators may explode, sending metal fragments into the cabin.
Reichel Foods Inc. is recalling Pro2Snax To The Max snack trays nationwide due to Listeria monocytogenes contamination.
Glenmark Pharmaceuticals is recalling Ranitidine Tablets USP 150 mg because testing detected the presence of the NDMA impurity.
Sym-Pac International Inc is recalling 2,000 cases of frozen Yellowfin Tuna Round Steaks after customer reports of illness and high histamine levels were identified.
Appco Pharma LLC is recalling Ranitidine Capsules 300 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).
Kalmar is recalling 2019 Ottawa T2E battery electric vehicles because electromagnetic interference can cause unexpected transmission shifting, increasing crash risk.
BMW is recalling specific X5 and X6 models because passenger air bag inflators may explode, posing a risk of serious injury or death.
AAA Pharmaceutical is recalling specific lots of Ranitidine 150 mg tablets because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).
Glenmark Pharmaceuticals is recalling Ranitidine Tablets USP 300 mg because the FDA detected the NDMA impurity in the product.
Triumph is recalling 2019-2020 Speed Twin motorcycles because the gear shift lever linkage may separate, potentially preventing gear changes and increasing crash risk.
Asclemed USA Inc. dba Enovachem Pharmaceuticals is recalling Estriol, USP, (Micronized), 0.06 g, due to out-of-specification impurity test results.
Glenmark Pharmaceuticals is recalling Ranitidine Tablets USP 150 mg because the product contains the NDMA impurity.
Five Star Gourmet Foods of Florida recalled Simply Fresh MiniMeals2Go Protein Packs because they may contain Listeria monocytogenes, a harmful bacteria.
BMW is recalling specific 2006-2015 models because driver air bag inflators may explode due to propellant degradation, posing a risk of serious injury or death.
Glenmark Pharmaceuticals is recalling Ranitidine Tablets USP 300 mg because the FDA detected the NDMA impurity in the product.
Five Star Gourmet Foods of Florida is recalling Simply Fresh MiniMeals2Go Avocado Toast snack packs because they may contain Listeria monocytogenes.
Winnebago is recalling 2020 Adventurer motorhomes because a heat coil may fail to disengage, increasing the risk of a fire.
Nestle Toll House Ultimate Turtle Delight Cookie Bars are being recalled due to the potential presence of food-grade rubber pieces.
AAA Pharmaceutical is recalling Ranitidine 150 mg tablets because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).
Glenmark Pharmaceuticals is recalling Ranitidine Tablets USP 300 mg because of the presence of the NDMA impurity.
Appco Pharma LLC is recalling specific lots of Ranitidine Capsules 150 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).
Glenmark Pharmaceuticals is recalling 217,956 bottles of Ranitidine Tablets USP 150 mg nationwide because the product contains the NDMA impurity.