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 deaths or serious injuries are reported, 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
Medline is recalling Suture Removal Trays because the Povidone-Iodine prep pads contain less iodine than the label claims.
Medline Industries is recalling 73 cases of Incision & Drainage Trays because the Povidone-Iodine prep pads contain less iodine than labeled.
Medline Industries is recalling sterile staple remover kits because the iodine concentration is below the labeled claim.
Medline Industries is recalling Suture Removal Packs because the iodine content is below the label claim of 0.85%.
Medline Industries is recalling IV Start Kits because the Povidone-Iodine prep pads contain less iodine than labeled.
Medline Industries is recalling Povidone-Iodine prep pads because the iodine content is below the labeled claim of 0.85%.
Medline is recalling 1,100 cases of GHS Suture Removal Trays because the iodine concentration is below the label claim.
Medline is recalling Incision and Drainage Tray Kits because the Povidone-Iodine prep pads contain less iodine than labeled.
Medline Industries is recalling Suture Removal Trays because the Povidone-Iodine prep pads contain less iodine than labeled.
Medline Industries is recalling Dressing Change Tray Kits because the Povidone-Iodine prep pads contain less iodine than the label claims.
Medline Industries is recalling Pediatric IV Kits because the Povidone-Iodine prep pads contain less iodine than labeled.
Medline Industries is recalling Vitrectomy CDS Packs because the iodine concentration is below the label claim of 0.85%.
Medline Industries is recalling Suture Removal Trays because the Povidone-Iodine prep pads contain less iodine than the label claims.
Medline is recalling Central Line Dressing Change Tray Kits because the iodine concentration in the prep pads is below the label claim.
Stryker is recalling Mistral-Air Premium Blankets because they may conduct electricity during high-energy defibrillation if applied upside down.
Medline Industries is recalling 80 cases of Wound Closure Trays because the iodine concentration in the prep pads is below the labeled claim of 0.85%.
Medline Industries is recalling suture removal trays because the povidone-iodine prep pads contain less iodine than labeled.
Medline Industries is recalling Suture Removal Kits because the iodine concentration is below the labeled claim of 0.85%.
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may have shifted during rework, potentially preventing proper assembly.
Medline Industries is recalling Skin Stapler RMVR trays because the iodine concentration in the prep pads is below the labeled claim.
Medline Industries is recalling RAD NECK ENT TRAY packs because the Povidone-Iodine prep pads contain subpotent iodine levels below the label claim.
Medline Industries is recalling Suture Removal Trays because the iodine concentration in the prep pads is below the labeled claim.
Medline Industries is recalling hip replacement kits containing Povidone-Iodine prep pads with iodine levels below the label claim of 0.85%.
Medline Industries is recalling IV Start Kits because the iodine concentration in the prep pads is below the labeled claim of 0.85%.
Medline Industries is recalling Suture Removal Kits because the iodine concentration is below the label claim of 0.85%.