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
Premier Produce is recalling one lot of Jicama Julienne contaminated with Listeria monocytogenes. The product was distributed to U.S. consignees.
A&H Focal Inc. is recalling Zhonghua Niubian tablets found to contain sildenafil, an unapproved drug for erectile dysfunction.
Medline is recalling Incision and Drainage Tray Kits because the Povidone-Iodine prep pads contain less iodine than labeled.
Medline Industries is recalling 60 cases of Anesthesia Kits because the Povidone-Iodine prep pads contain less iodine than the label claims.
Medline Industries is recalling Suture Removal Kits because the iodine concentration is below the label claim.
A&H Focal Inc. is recalling Tiger King tablets because they contain sildenafil, an unapproved drug for erectile dysfunction, and lack FDA approval.
Medline Industries is recalling IV Start Kits because the iodine concentration in the prep pads is below the labeled claim.
Medline Industries is recalling sterile incision and drainage tray kits because the povidone-iodine prep pads contain less iodine than labeled.
A&H Focal Inc. is recalling HU HU SHENG WEI capsules because FDA analysis found they contain sildenafil, an unapproved drug for which safety and efficacy have not been established.
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 IV Start Kits because the iodine concentration in the prep pads is below the labeled claim of 0.85%.
The FDA is recalling ZHANSHENG WEIGE CHAOYUE XILISHI tablets because they contain sildenafil, an unapproved drug for which safety and efficacy have not been established.
Medline Industries is recalling I&D Tray Kits because the Povidone-Iodine prep pads contain less iodine than the label claims.
Medline Industries is recalling sterile Povidone-Iodine prep pads because the iodine content is below the labeled 0.85% claim.
Medline Industries is recalling Circumcision Tray Kits because the iodine concentration in the prep pads is below the labeled claim.
A&H Focal Inc. is recalling DADIYONGSHI XIANGGANGTIANLONGSHENGWU tablets because they contain sildenafil, an unapproved drug for erectile dysfunction.
Medline Industries is recalling CNTRL Line Removal Kit Scripps because the iodine content is below the label claim.
Medline Industries is recalling Suture Removal Kits 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.
A&H Focal Inc. is recalling Hard Ten Days capsules because they contain sildenafil, an unapproved drug for which safety and efficacy have not been established.
A&H Focal Inc. is recalling MACA gold tablets sold in New York and New Jersey because they contain sildenafil, an unapproved drug.
Medline Industries is recalling Abdominal Surgery II Packs because the iodine content in the prep pads is below the label claim.
Medline Industries is recalling Skin Stapler RMVR trays because the iodine concentration in the prep pads is below the labeled claim.
Medline is recalling Incision and Drainage Trays 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%.