Class II medical devices recalls – page 50

• BD PhaSeal Injector Luer (N30C) recall
  FDA September 3, 2025 · Bd Switzerland Sarl · Class II
• The Medline General Surgery Tray is customized to meet requirements of the… recall
  FDA September 3, 2025 · Medline Industries, LP · Class II
• Orascoptic Superior Visualization Phantom Nose Pad Accessory Kit ( nose… recall
  FDA September 3, 2025 · Orascoptic Surgical Acuity · Class II
• Orascoptic Superior Visualization Dragonfly Nose Pad Accessory Kit ( nose… recall
  FDA September 3, 2025 · Orascoptic Surgical Acuity · Class II
• Orascoptic Superior Visualization Phantom Essential kit ( Nose pad… recall
  FDA September 3, 2025 · Orascoptic Surgical Acuity · Class II
• Orascoptic Superior Visualization Dragonfly Essentials Kit ( Nose pad… recall
  FDA September 3, 2025 · Orascoptic Surgical Acuity · Class II
• Orascoptic Superior Visualization Custom loupes configured with Phantom… recall
  FDA September 3, 2025 · Orascoptic Surgical Acuity · Class II
• Orascoptic Superior Visualization Custom loupes with Dragonfly frames recall
  FDA September 3, 2025 · Orascoptic Surgical Acuity · Class II
• TherMax Blood Warmer Unit-US, PrisMax Accessory, Product Codes: 955630… recall
  FDA September 3, 2025 · Vantive Us Healthcare LLC · Class II
• PrisMax V3 control Unit-US, Hemodialysis Delivery System… recall
  FDA September 3, 2025 · Vantive Us Healthcare LLC · Class II
• PrisMax V2-US, Hemodialysis Delivery System, Product Codes: 955626… recall
  FDA September 3, 2025 · Vantive Us Healthcare LLC · Class II
• ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS STEM EXTENSION, STRAIGHT… recall
  FDA September 3, 2025 · Onkos Surgical, Inc. · Class II
• ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS SEGMENTAL STEM CANAL FILLING… recall
  FDA September 3, 2025 · Onkos Surgical, Inc. · Class II
• ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS BOWED CANAL FILLING STEMS… recall
  FDA September 3, 2025 · Onkos Surgical, Inc. · Class II
• Atlantis IO FLO Product Name: Atlantis IO FLO-S Kit Model recall
  FDA September 3, 2025 · Dentsply IH, Inc. · Class II
• Atlantis IO FLO-S Product Name: Atlantis IO FLO-S Kit Model recall
  FDA September 3, 2025 · Dentsply IH, Inc. · Class II
• Corin Operating Tables Model Numbers: (1) 770001A0, (2) 770001A2… recall
  FDA September 3, 2025 · Maquet Gmbh · Class II
• THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model recall
  FDA September 3, 2025 · THOR Photomedicine Ltd · Class II
• THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model recall
  FDA September 3, 2025 · THOR Photomedicine Ltd · Class II
• THOR Product Name: NovoTHOR XL Model recall
  FDA September 3, 2025 · THOR Photomedicine Ltd · Class II
• THOR Product Name: NovoTHOR Model recall
  FDA September 3, 2025 · THOR Photomedicine Ltd · Class II
• Spectrum IQ Infusion Pump, Product Code 3570009 recall
  FDA September 3, 2025 · Baxter Healthcare Corporation · Class II
• GE HealthCare OEC 9900 Elite C-arm Systems recall
  FDA September 3, 2025 · GE Medical Systems, LLC · Class II
• GE HealthCare OEC 9800 recall
  FDA September 3, 2025 · GE Medical Systems, LLC · Class II
• Dynex Agility Sample Tips recall
  FDA August 27, 2025 · Dynex Technologies, Inc. · Class II
• OtoLase Starter Kit recall
  FDA August 27, 2025 · Lumenis, Ltd. · Class II
• Burr Hole Cover Kit recall
  FDA August 27, 2025 · Boston Scientific Neuromodulation Corporation · Class II
• Electrosurgical, Cutting and Coagulation and Accessories recall
  FDA August 27, 2025 · Olympus Corporation of the Americas · Class II
• Electrosurgical, Cutting and Coagulation and Accessories recall
  FDA August 27, 2025 · Olympus Corporation of the Americas · Class II
• Clearview Strep A Exact II Dipstick Respiratory Kit, CLIA Waived recall
  FDA August 27, 2025 · Mckesson Medical-Surgical Inc. Corporate Office · Class II
• Estrone RIA recall
  FDA August 27, 2025 · Immunotech A.S. · Class II
• VITROS Chemistry Products Ca Slides recall
  FDA August 27, 2025 · Ortho-Clinical Diagnostics, Inc. · Class II
• Injection needle, bayonet, Luer-Lock, 1. Model no recall
  FDA August 27, 2025 · Spiggle & Theis Mt Gmbh · Class II
• Q-Stop Product Name: Suture Retention Device Model recall
  FDA August 27, 2025 · Drs Vascular, Inc · Class II
• Pentax Medical Video Processor recall
  FDA August 27, 2025 · Pentax of America Inc · Class II
• HemosIL LMW Heparin Controls recall
  FDA August 20, 2025 · Instrumentation Laboratory · Class II
• Access Thyroglobulin assay, a simultaneous one-step immunoenzymatic assay recall
  FDA August 20, 2025 · Beckman Coulter, Inc. · Class II
• GE SIGNA PET/MR AIR Plus (China Only), Nuclear Magnetic Resonance Imaging… recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA PET/MR AIR (China Only), Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA Hero MAX (China Only), Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA Hero Elite (China Only), Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA Hero XT (China Only), Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA Premier MAX (China Only), Nuclear Magnetic Resonance Imaging… recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA Premier Elite (China Only), Nuclear Magnetic Resonance Imaging… recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA Premier XT (China Only), Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA Architect AIR (China Only), Nuclear Magnetic Resonance Imaging… recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA Voyager AIR (China Only), Nuclear Magnetic Resonance Imaging… recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA Artist Evo, Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA PET/MR, Tomographic Imager Combining Emission Computed Tomography… recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA Hero, Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE Discovery MR750w 3.0T, Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE Discovery MR750 3.0T, Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA UHP, Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA Premier, Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE SIGNA Architect, Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE Optima MR450w 1.5T, Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE Discovery MR450 1.5T, Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE Signa Voyager, Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• GE Signa Artist, Nuclear Magnetic Resonance Imaging System recall
  FDA August 20, 2025 · GE Medical Systems, LLC · Class II
• Ultra IABP Catheter Kit Product Name: Ultra IABP Catheter Kit Model recall
  FDA August 20, 2025 · Insightra Medical Inc · Class II