Class II medical devices recalls – page 11

• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H… recall
  FDA July 1, 2026 · Boston Scientific Corporation · Class II
• Philips Telemetry Monitor 5500 1.4 GHz recall
  FDA July 1, 2026 · Philips North America Llc · Class II
• Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral… recall
  FDA July 1, 2026 · Zimmer, Inc. · Class II
• Octopus 4 Tissue Stabilizer, Model 29400 recall
  FDA July 1, 2026 · Medtronic Perfusion Systems · Class II
• Octopus Evolution AS Tissue Stabilizer, Model TS2500 recall
  FDA July 1, 2026 · Medtronic Perfusion Systems · Class II
• Octopus Evolution Tissue Stabilizer, Model TS2000 recall
  FDA July 1, 2026 · Medtronic Perfusion Systems · Class II
• Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 US… recall
  FDA July 1, 2026 · Dexcom, Inc. · Class II
• Surgify Halo, 5.4 mm, Long, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Long, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Long, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Long, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Medium, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Medium, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Short, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Short, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Extendable, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Extendable, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 40 mm, Long, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 4.0 mm, Short, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 4.0 mm, Short, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 4.0 mm, Short, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 4.0 mm, Extendable, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 4.0 mm, Extendable, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 3.0 mm, Long, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 3.0 mm, Short, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 3.0 mm, Extendable, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Thuvera Laser Console recall
  FDA July 1, 2026 · IPG Medical Corporation · Class II
• GE Healthcare AW Server 3.2 ext.6.5 recall
  FDA July 1, 2026 · GE Medical Systems SCS · Class II
• INZONE DETACHMENT SYSTEM recall
  FDA July 1, 2026 · Stryker Neurovascular · Class II
• Acumed Hexalob Screw various sizes recall
  FDA July 1, 2026 · Acumed LLC · Class II
• Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide, Model recall
  FDA July 1, 2026 · Zimmer, Inc. · Class II
• Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide, Model recall
  FDA July 1, 2026 · Zimmer, Inc. · Class II
• Off-Axis Comprehensive Shoulder System, Large, Augment, Off-Axis… recall
  FDA July 1, 2026 · Zimmer, Inc. · Class II
• Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis… recall
  FDA July 1, 2026 · Zimmer, Inc. · Class II
• Off-Axis Comprehensive Shoulder System Small, Augment, Off-Axis… recall
  FDA July 1, 2026 · Zimmer, Inc. · Class II
• Multi-Snare Set: 5 mm x 125 cm recall
  FDA July 1, 2026 · Pfm Medical Inc. · Class II
• VOCSN+Pro package recall
  FDA July 1, 2026 · Ventec Life Systems, Inc. · Class II
• TMJ Bilateral Implants recall
  FDA July 1, 2026 · TMJ Solutions Inc · Class II
• Philips Avalon Fetal Monitor, FM 30 Part numberM2703A recall
  FDA July 1, 2026 · Philips North America Llc · Class II
• Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A recall
  FDA July 1, 2026 · Philips North America Llc · Class II
• Da Vinci ASSY, PSS, SP1098, Part Number: 380601 recall
  FDA July 1, 2026 · Intuitive Surgical, Inc. · Class II
• HeartMate Product Name: HM 11V Li-ion Backup Battery, ABT Model recall
  FDA June 24, 2026 · Thoratec LLC · Class II
• HeartMate Product Name: HeartMate 3" System Controller Model recall
  FDA June 24, 2026 · Thoratec LLC · Class II
• HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits… recall
  FDA June 24, 2026 · Thoratec LLC · Class II
• Splashwire Hydrophilic Guide Wire recall
  FDA June 24, 2026 · Merit Medical Systems, Inc. · Class II
• Inspire Medical Systems, Inc recall
  FDA June 24, 2026 · Inspire Medical Systems Inc. · Class II
• Inspire Medical Systems, Inc recall
  FDA June 24, 2026 · Inspire Medical Systems Inc. · Class II
• BD Connecta" BD Luer-Lok" 360 recall
  FDA June 24, 2026 · Bd Switzerland Sarl · Class II