Class IIOngoingZ-2633-2026
Boston Scientific Corporation recalls CRE Wireguided 8-10mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
Boston Scientific Corp…MAJul 8, 2026
All device recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 469–480 of 4,996 recalls
Class IIOngoingZ-2632-2026
Boston Scientific Corporation recalls CRE Wireguided 6-8mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
Boston Scientific Corp…MAJul 8, 2026
Class IIOngoingZ-2631-2026
Boston Scientific Corporation recalls CRE Pro Wireguided 18-20mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
Boston Scientific Corp…MAJul 8, 2026
Class IIOngoingZ-2630-2026
Boston Scientific Corporation recalls CRE Pro Wireguided 15-18mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
Boston Scientific Corp…MAJul 8, 2026
Class IIOngoingZ-2629-2026
Boston Scientific Corporation recalls CRE Pro Wireguided 12-15mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
Boston Scientific Corp…MAJul 8, 2026
Class IIOngoingZ-2628-2026
Boston Scientific Corporation recalls CRE Pro Wireguided 10-12mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
Boston Scientific Corp…MAJul 8, 2026
Class IIOngoingZ-2627-2026
Boston Scientific Corporation recalls CRE Pro Wireguided 8-10mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
Boston Scientific Corp…MAJul 8, 2026
Class IIOngoingZ-2626-2026
Boston Scientific Corporation recalls CRE Pro Wireguided 6-8mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
Boston Scientific Corp…MAJul 8, 2026
Class IIOngoingZ-2625-2026
Hamilton Medical AG recalls IntelliCuff
Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the cuff pressure set by the user.
Hamilton Medical AGJul 8, 2026
Class IOngoingZ-2624-2026
Medtronic Heart Valves Division recalls Medtronic Harmony Delivery Catheter System
Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system under certain procedural or anatomical conditions due to a man…
Medtronic Heart Valves…CAJul 8, 2026
Class IIOngoingZ-2623-2026
Remel, Inc recalls GC Agar Base (150mm) 10/PK R04030
Reduced or no recovery of some strains of Neisseria gonorrhoeae.
Remel, IncKSJul 8, 2026
Class IOngoingZ-2622-2026
Windstone Medical Packaging, Inc. recalls A M S
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
Windstone Medical Pack…MTJul 8, 2026