Recalls & alerts

602 alerts recorded, refreshed every six hours. Filter by source or category.

• openFDA · August 19, 2026Moderate risk

  Cardinal Health 200, LLC : Cardinal Health Presource Kits: 1) ENT TRAY , Catalog Number: 24-0726A; 2) KIT,SINUS , Catalog Number: PE13SPAJA; 3) KIT,SINUS , Catalog Number: PE13SPAJB; 4)…

  Cardinal Health Presource Kits, including ENT, sinus, nasal septoplasty, head and neck, nasal, and EENT trays with specific catalog numbers, are affected. The kits contain MEDICOM Ritmed Neurological Sponges with unexpected variability in endotoxin levels, exposing patients to potential harm. Consumers should stop using these kits and contact Cardinal Health for return or replacement instructions.

  devices
• openFDA · August 19, 2026Moderate risk

  W L Gore & Associates, Inc. : GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VSWVN1010. Flexible, self-expanding endoprosthesis designed to maintain luminal patency of the common…

  The recall affects GORE VIABIL Biliary Endoprosthesis, Model VSWVN1010, distributed in Georgia and Rhode Island. The device is mislabeled, containing a 10 mm x 7 cm stent with drainage holes instead of the 10 mm x 10 cm version without holes,

  devices

Data comes from official CPSC and FDA publications (United States). Summaries are generated automatically from those publications: the cited source prevails.