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
The FDA is recalling 3,113,280 units of the EGIA 30 Articulating Medical device due to missing pin components that may cause incomplete staple formation and serious surgical complications.
The FDA is recalling 3,113,280 units of EGIA45 CT AR MD THK REL surgical staplers because missing pin components may cause incomplete staple formation, leading to serious surgical complications.
Grandma's Fireworks is recalling 18 types of consumer fireworks because they are overloaded with pyrotechnics, posing explosion and burn risks.
The FDA is recalling Signia Tri-Staple 2.0 devices because missing pin components may cause incomplete staple formation, leading to serious surgical complications.
P & L Developments, LLC is recalling 202,068 bottles of Cetirizine HCL Oral Solution due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.
Ethicon, Inc. is recalling specific lots of ETHIBOND EXCEL polyester sutures because raw materials may contain high endotoxin levels.
The FDA is recalling 3,113,280 units of the EGIA 45 Articulating Xtra Thick Sulu device due to a missing pin component that may cause incomplete staple formation and serious medical complications.
Zydus Pharmaceuticals USA Inc. is recalling Pramipexole Dihydrochloride Tablets 1.5 mg due to cross-contamination caused by cleaning failures.
GE Healthcare is recalling 1,113 Discovery IQ PET/CT systems because the table may stop moving while X-ray exposure continues.
Cook Inc. is recalling 73 Advance Enforcer 35 Focal Force PTA Balloon Catheters because they may burst below the rated pressure, posing risks of vessel injury and balloon fragmentation.
Cook Inc. is recalling 34 Advance Enforcer 35 Focal Force PTA Balloon Catheters because they may burst below the rated pressure, posing risks of vessel injury and balloon fragmentation.
FDA is recalling 3,113,280 units of the EGIA 60 Curved Tip Art Med Thick Sulu surgical stapler because missing pin components may cause incomplete staple formation and serious medical complications.
GE Healthcare is recalling 1,113 Optima PET/CT 560 and 560FX systems because the table may stop moving while X-ray exposure continues.
Preferred Pharmaceuticals is recalling specific lots of Robafen DM cough syrup due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.
Charles Machine is recalling 2018-2019 Ditch Witch trailers because hitch lock nuts may fail to clamp the load, increasing crash risk.
Daimler Vans USA is recalling 2018-2019 Mercedes-Benz Metris vehicles because a steering sensor defect may cause the electric power steering assist to deactivate, increasing crash risk.
San Giuseppe Salami Co. by Giacomo is recalling approximately 832 pounds of frozen andouille sausage due to possible metal contamination. No illnesses have been reported.
Mazda is recalling 2010-2011 RX-8 vehicles because the passenger air bag inflator may explode during deployment, potentially causing serious injury or death.
Oshkosh is recalling 2019 McNeilus Meridian, Atlantic, and Contender front loader trucks because battery cables may rub against the fuse box bracket, increasing the risk of fire.
Oshkosh is recalling 2018 McNeilus Bridgemaster V Concrete Mixers because an incorrect filler neck part may cause the tank to overpressurize and rupture.
Altec is recalling 2003-2019 aerial devices due to potential air brake pressure loss. Owners should contact dealers for free inspection and repair.
Spartan Motors is recalling 4,534 Utilimaster Walk-In Vans because a brake pedal clip may detach, causing brake light failure or pedal detachment.
Oshkosh is recalling 2018-2019 S-Series Mixer vehicles because hydraulic hoses may be installed incorrectly, causing loss of steering assist and increasing crash risk.
TRW is recalling air bag electronic control units that may malfunction, potentially disabling or unexpectedly deploying air bags and seat belt pretensioners.
Heritage Pharmaceuticals is recalling Prochlorperazine Edisylate Injection because microbial growth was detected in a sublot. The affected vials are distributed nationwide.