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
Draeger is recalling 14,420 ErgoStar CM 40 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen karela ring cut after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Draeger is recalling 191,470 ErgoStar CM 45 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen tindora after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen red guava slices after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen chauri after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Medline is recalling 163 DEXLOCK Achilles Repair Implant Kits after multiple complaints of the drill bit fusing to the bushing within the drill guide during use.
Autocar is recalling one 2024 E-ACTT terminal tractor because improperly secured battery cable connections may overheat and cause a fire or loss of motive power.
Suzuki is recalling 2025-2026 DR-Z400S and 2025 DR-Z400SM motorcycles because incorrectly tightened screws may allow brake fluid to leak, reducing braking ability.
Steris is recalling 22 AMSCO 7053HP Washer/Disinfectors because a wire connected to the electrical box may shift out of position, which may result in electrical arcing inside the unit.
Toyota is recalling certain 2024-2025 Highlander and Highlander Hybrid vehicles because the third row centre seat belt roof anchor may have been installed at an incorrect angle.
BMW is recalling specific 2014-2015 2, 3, and 4 Series vehicles because the head air bag inflator may fail, posing an injury risk during a crash.
Orthofix U.S. is recalling 34,582 FORZA PTC Spacer System units because the labeling contains claims that are not consistently present.
Glenmark Pharmaceuticals is recalling 672 bottles of Nebivolol Tablets, 20 mg, over cross contamination with other products.
Medline is recalling 11,291,800 Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", because packaging may exhibit open seals that could compromise the sterility of the product.
Waldemar Link is recalling 18 Endo Model Knee Fusion Nail SK coupling components delivered with a preassembled locking screw inserted from the wrong side into the male taper.
Cipla USA is recalling 15,744 bottles of Cinacalcet Hydrochloride Tablets, 60 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.
Cipla USA is recalling Lanthanum Carbonate chewable tablets, 1000mg, after the product failed stability specifications with an out of specification hardness test result.
Rollx Vans is recalling certain converted vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints, because the retractors may not lock and the wheelchair may not be properly secured.
Medline is recalling 18,000 units of Curad Quick Strip Fabric Bandages because packaging may exhibit open seals that could compromise the sterility of the product.
Medline is recalling 1,566,500 Fur Friends Plastic Sterile Adhesive Bandages because packaging may exhibit open seals that could compromise the sterility of the product.
Bard Peripheral Vascular is recalling 1,240 Safe-T-Centesis 6 Fr Catheter Drainage Trays because the safety indicator can show the catheter in the sharp position when it is blunt.
Cipla USA is recalling 63,504 bottles of Cinacalcet Hydrochloride Tablets, 30 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.
Medline is recalling 4,381,400 Quick Strip Plastic Sterile Adhesive Bandages because packaging may exhibit open seals that could compromise the sterility of the product.
Chetak New York is recalling Deep-brand frozen jamun after the product tested positive for Salmonella. The FDA has classified the action as Class I.