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
Centurion Medical Products is recalling specific tracheostomy care kits and trays because incomplete seals may compromise sterility.
Centurion Medical Products Corporation is recalling specific sterile medical packs and trays because incomplete seals may compromise sterility.
Centurion Medical Products is recalling 1,986 circumcision trays because incomplete seals on the sterile packaging may compromise sterility.
Cardinal Health is recalling AAMI 3 nonreinforced surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Zimmer Biomet is recalling three units of the Coonrad/Morrey Total Elbow Humeral Assembly because the lot contained two outer pins instead of one outer and one inner pin.
Centurion Medical Products Corporation is recalling specific lots of sterile surgery kits because incomplete seals may compromise sterility.
Centurion Medical Products is recalling specific surgical trays because incomplete seals on the sterile packages may compromise sterility.
Centurion Medical Products is recalling 1,820 sterile nasal speculums due to incomplete package seals that may compromise sterility.
Cardinal Health is recalling AAMI 3 ROYALSILK SURGGOWN BNS XL units worldwide due to unknown levels of bioburden, microbiological flora, and particulate contamination.
B. Braun Medical is recalling 2,736 Y-Type Blood Sets due to a potential for leakage at the joint between the blood filters and tubing.
Centurion Medical Products Corporation is recalling sterile uterine sounds because incomplete seals may compromise sterility. The products were distributed nationwide and in Ghana.
Centurion Medical Products is recalling 60 Biopsy Trays because incomplete seals on the sterile package may compromise sterility.
Centurion Medical Products is recalling 108 units of Skin Prep Kits due to incomplete seals that may compromise sterility.
Cardinal Health is recalling specific lots of AAMI 3 surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Cook Inc. is recalling Universa Soft Ureteral Stents because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into patients instead of the flexible tip.
Cook Inc. is recalling 13,388 Percutaneous Malecot Nephrostomy Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into patients instead of the flexible tip.
Cardinal Health is recalling AAMI 3 Non-Reinf Surgical Gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Roche Diabetes Care is recalling Accu-Chek Aviva Plus test strips because they may fail to dose, potentially delaying treatment decisions.
Cook Inc. is recalling Bentson PTFE Wire Guides because they may be incorrectly loaded, causing the stiff tip to be introduced into patients instead of the flexible tip.
Clinical Diagnostic Solutions is recalling Medonic M-Series Hematology Analyzers due to a risk of sample misidentification and operator injury from exposed needles.
Cook Inc. is recalling Sof-Flex Double Pigtail Ureteral Stent Sets because the wire guide may be incorrectly loaded, potentially introducing a stiff tip into the patient.
Cook Inc. is recalling Kwart Retro-Inject Ureteral Stent Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into the patient instead of the flexible tip.
B. Braun Medical is recalling 1,824 Outlook Safety Infusion System Y-type Blood Sets due to a potential for leakage at the joint between the blood filters and tubing.
Datascope is recalling specific lots of Reinforced Introducer Sets because breached pouches may have compromised sterility.
Centurion Medical Products Corporation is recalling specific sterile surgical trays because incomplete seals may compromise sterility. The affected products were distributed nationwide and in Ghana.