Recalls distributed in Florida – page 4

• COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model recall
  FDA August 12, 2026 · Tissium Sa · Class II
• COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model recall
  FDA August 12, 2026 · Tissium Sa · Class II
• COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model recall
  FDA August 12, 2026 · Tissium Sa · Class II
• COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model recall
  FDA August 12, 2026 · Tissium Sa · Class II
• COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model recall
  FDA August 12, 2026 · Tissium Sa · Class II
• COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model recall
  FDA August 12, 2026 · Tissium Sa · Class II
• COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model recall
  FDA August 12, 2026 · Tissium Sa · Class II
• COAPTIUM Connect Product Name: COAPTIUM Connect Model recall
  FDA August 12, 2026 · Tissium Sa · Class II
• GEM Premier 5000 PAK Part Numbers: 00055360010 00055360011 00055407504… recall
  FDA August 12, 2026 · Instrumentation Laboratory · Class II
• GEM Premier 7000 with iQM3 Part Numbers: 00077407508 00077407510… recall
  FDA August 12, 2026 · Instrumentation Laboratory · Class II
• REF # D23354, MicroScan LabPro V5.03 Panel Update 11 DVD Kit (US) on the… recall
  FDA August 12, 2026 · Beckman Coulter, Inc. · Class II
• REF # D23352, MicroScan LabPro V5.03 Panel Update 11 (US)… recall
  FDA August 12, 2026 · Beckman Coulter, Inc. · Class II
• HardyDisk AST Cefiderocol 30¿g (FDC30) recall
  FDA August 12, 2026 · Hardy Diagnostics · Class II
• FilmArray NGDS Warrior Panel recall
  FDA August 12, 2026 · Biofire Defense · Class II
• Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40… recall
  FDA August 12, 2026 · Maquet Critical Care AB · Class II
• OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model recall
  FDA August 12, 2026 · Oxos Medical Inc · Class II
• munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control… recall
  FDA August 12, 2026 · Munevo Gmbh · Class II
• Quantum Rehab Product Name: Quantum Rival Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: 4Front Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Quantum 4Front 2HD Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Q6 Edge 4 Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Q6 Edge 3 Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Q6 Edge 2.0 (ilevel) Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Quantum 1450 Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum rehab Product Name: Q6 Edge 2.0 Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Q6 Edge HD Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: R-TRAK Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Q6 Edge 3 Stretto Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Quantum Outback Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Quantum 4Front 2 Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN:… recall
  FDA August 12, 2026 · Boston Scientific Corporation · Class II
• Radial Jaw 4 Large Capacity Biopsy Forceps with the following descriptions… recall
  FDA August 12, 2026 · Boston Scientific Corporation · Class II
• Radial Jaw 4 Standard Capacity Biopsy Forceps with the following… recall
  FDA August 12, 2026 · Boston Scientific Corporation · Class II
• REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The… recall
  FDA August 12, 2026 · Beckman Coulter Biomedical GmbH · Class II
• Stryker Hoffmann II Connecting Rod Micro 3 x 150mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• Stryker Hoffmann II Connecting Rod Micro 3 x 120mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• Stryker Hoffmann II Connecting Rod Micro 3 x 90mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• Stryker Hoffmann II Connecting Rod Micro 3 x 60mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• Stryker Hoffmann II Connecting Rod Micro 3 x 50mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• Stryker Hoffmann II Connecting Rod Micro 3 x 40mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• Stryker Hoffmann II Connecting Rod Micro 3 x 30mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Port… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Loop… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Block… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Heart… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Angio… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1)… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Dr… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: SPINAL… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• M5 Corpus Power Wheelchair recall
  FDA August 5, 2026 · Permobil Inc · Class II
• L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm recall
  FDA August 5, 2026 · Argon Medical Devices, Inc · Class II
• L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm… recall
  FDA August 5, 2026 · Argon Medical Devices, Inc · Class II
• Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock recall
  FDA August 5, 2026 · Permobil Inc · Class II
• Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that… recall
  FDA August 5, 2026 · ResMed Ltd. · Class I
• Flexible Hystero-Fiberscope Kits recall
  FDA July 29, 2026 · Karl Storz Endoscopy · Class II
• Medline medical convenience kits labeled as: 1) TOTAL JOINT PACK Medline… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits labeled as: NEURO PACK… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits labeled as: 1) SHOULDER PACK… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits labeled as: 1) KIT PEDIATRIC OPEN HEART… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II