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
Daring Foods is recalling Plant Steak Bites because the packaging can rupture or explode during cooking. The product was distributed to six retail locations in Florida and North Carolina.
Beckman Coulter is recalling DxU 840m and 850m Iris analyzers because a check valve defect can cause fluid leaks, creating slip, chemical, and biohazard risks.
Medtronic is recalling 18 units of Grafton DBM and Grafton Plus DBM products because the donor tissue tested positive for Clostridium butyricum, posing a potential infection risk.
Ethicon is recalling 1,764 units of PERMA-HAND Silk sutures that were packaged with alcohol-based fluid. The fluid is not part of the product design and could cause surgical delays or treatment failure if used.
Zydus Pharmaceuticals is recalling 70,776 vials of Hydrocortisone Sodium Succinate for Injection due to failed impurities and degradation specifications.
Steris Corporation is recalling 374 units of RAPICIDE PA Part A High-Level Disinfectant because a blocked vented cap may cause the bottle to swell and release vapor or liquid, posing an injury risk.
Houston Rx LLC is recalling 64 vials of Tirzepatide/Niacinamide injection due to a lack of assurance of sterility. The product was distributed nationwide.
Medline is recalling 56 surgical convenience kits because the cannula components may leak or break during use.
Steris is recalling 11,806 units of its RAPICIDE PA high-level disinfectant because a blocked vented cap can cause the bottle to swell and release vapor or liquid, risking user injury.
Medline Industries is recalling 36,199 surgical convenience kits nationwide because cannula components do not meet ISO 80369-7 dimensional requirements, posing a risk of leaking or breaking during use.
Becton Dickinson is recalling 669,200 units of the BD Phoenix Panel NMIC-306 due to potential quality control failures with Klebsiella pneumoniae ATCC BAA-1705.
Hyundai is recalling 2026 Venue, Elantra N, Elantra Hybrid, and Elantra vehicles because wheel lug nuts may loosen, allowing the wheel to detach.
Cadwell Industries is recalling 23 IOMAX Cortical Modules because a defective circuit board may cause unintended electrical stimulation to patients.
General Motors is recalling 2026 Chevrolet Traverse and GMC Acadia vehicles because insufficient seat welds may fail to restrain occupants in a crash.
Audi is recalling 2024-2025 Q4 E-Tron and Q4 Sportback E-Tron vehicles because the high-voltage battery may fail and cause a fire.
Jenavalve Technology Inc. is recalling 111 units of JenaValve Trilogy Delivery Catheters due to a defect that may prevent heart valve deployment.
Deano's Pasta is recalling Pear and Pecorino Triangoli Ravioli because the product contains undeclared lobster, a major food allergen.
Instrumentation Laboratory is recalling 1,414 units of HemoslL AcuStar HIT-lgG(PF-4) in vitro diagnostic reagents due to a potential for invalid calibration curves or negative mean bias of up to 47% with patient samples.
BMW is recalling certain 2018-2020 530e and 740Le vehicles because a loose positive battery cable on the engine starter can spark and cause a fire.
Jenavalve Technology Inc. is recalling 108 units of the JenaValve Trilogy Delivery Catheter due to a defect that may prevent heart valve deployment.
Medtronic is recalling specific Grafton DBM and Grafton Plus DBM products because the donor tissue tested positive for Clostridium butyricum, posing a potential infection risk.
Beckman Coulter is recalling IQ200 SPRINT, SELECT, and ELITE hematology analyzers because a check valve defect may cause fluid leaks, creating slip, chemical, and biohazard risks.
Medline is recalling 193,374 surgical convenience kits nationwide because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.
Medline Industries is recalling 1,900 surgical convenience kits because cannula components do not meet ISO 80369-7 standards and may leak or break during use.
Saratoga Potato Chips LLC is recalling J. HIGGS Loaded Bacon & Cheddar Potato Chips due to undeclared soy. The product was sold in Save A Lot stores in six states.