Nationwide recalls – page 10

• 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
• Kingfisher Compact Individual First Aid Kit recall
  FDA August 12, 2026 · Integrated Medcraft LLC · Class II
• FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12) recall
  FDA August 12, 2026 · Integrated Medcraft LLC · Class II
• Charger for the Therabody Theragun, G4 PRO massage device… recall
  FDA August 12, 2026 · Therabody, Inc · Class II
• Halyard convenience kits containing recalled Medline Namic Angiographic… recall
  FDA August 12, 2026 · AVID Medical, Inc. · Class I
• Halyard convenience kits containing recalled Medline Namic Angiographic… recall
  FDA August 12, 2026 · AVID Medical, Inc. · Class I
• Halyard convenience kits containing recalled Medline Namic Angiographic… recall
  FDA August 12, 2026 · AVID Medical, Inc. · Class I
• Ashfiat Alharamain Energy Support 250ml/8fl recall
  FDA August 12, 2026 · Akkarco LLC · Class I
• Mirabegron Extended-Release Tablets, 25 mg, 30-count bottle, Rx only… recall
  FDA August 12, 2026 · Zydus Pharmaceuticals (USA) Inc · Class II
• Cyclophosphamide for Injection, USP, 2 gram/vial, One Single-Dose Vial… recall
  FDA August 12, 2026 · Sunny Pharmtech Inc. · Class I
• Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial… recall
  FDA August 12, 2026 · Sunny Pharmtech Inc. · Class I
• Dicyclomine Hydrochloride Capsules, USP, 10mg, 1,000 bottles, Rx only… recall
  FDA August 12, 2026 · Aurobindo Pharma USA Inc · Class II
• Wichard Groupe North America Recalls Courant Spliced Kalimba Climbing Ropes Due to Risk of Serious Injury or Death from Fall Hazard
  CPSC August 6, 2026 · Wichard Groupe North America
• KC Imports and Exports Recalls Mini Laser Pointer Keychains Due to Risk of Serious Injury or Death from Battery Ingestion…
  CPSC August 6, 2026 · KC Imports and Exports
• Louisville Ladder Recalls Over One Million Attic Stairway Ladders Due to Risk of Serious Injury or Death from Fall Hazard
  CPSC August 6, 2026 · Louisville Ladder
• DR Power Equipment Recalls Lawn Mowers Due to Risk of Serious Injury or Death from Laceration Hazard…
  CPSC August 6, 2026 · DR Power Equipment
• 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
• GEM Premier 5000 Product Name: GEM Premier 5000 Model recall
  FDA August 5, 2026 · Instrumentation Laboratory · Class II
• GEM Premier 5000 Product Name: GEM Premier 5000 Model recall
  FDA August 5, 2026 · Instrumentation Laboratory · Class II
• GEM Premier 5000 Product Name: GEM Premier 5000 Model recall
  FDA August 5, 2026 · Instrumentation Laboratory · Class II
• GEM Premier 5000 Product Name: GEM Premier 5000 Model recall
  FDA August 5, 2026 · Instrumentation Laboratory · Class II
• GEM Premier 7000 with iQM3 Product Name: GEM Premier 7000 with iQM3 Model recall
  FDA August 5, 2026 · Instrumentation Laboratory · Class II
• GEM Premier 5000 with IQM2 Model recall
  FDA August 5, 2026 · Instrumentation Laboratory · Class II
• OsteoBallast, 45 x 17.5 mm (SeaSpine Brand) recall
  FDA August 5, 2026 · IsoTis OrthoBiologics, Inc. · 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
• EOPA 3D Arterial Cannula 22FR, intended for use with cardiopulmonary… recall
  FDA August 5, 2026 · Medtronic Perfusion Systems · Class II
• EOPA 3D Arterial Cannula DIL TIP 22FR, intended for use with… recall
  FDA August 5, 2026 · Medtronic Perfusion Systems · Class II
• EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR… recall
  FDA August 5, 2026 · Medtronic Perfusion Systems · Class II
• EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR… recall
  FDA August 5, 2026 · Medtronic Perfusion Systems · Class II
• EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR… recall
  FDA August 5, 2026 · Medtronic Perfusion Systems · Class II
• EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR… recall
  FDA August 5, 2026 · Medtronic Perfusion Systems · Class II
• M5 Corpus Power Wheelchair recall
  FDA August 5, 2026 · Permobil 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)… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock recall
  FDA August 5, 2026 · Permobil Inc · Class II
• Power Over Fiber Base Module recall
  FDA August 5, 2026 · Terex Utilities · Class II
• Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that… recall
  FDA August 5, 2026 · ResMed Ltd. · Class I
• Ingenuity CT CT5000 Ingenuity Plus CT5000 Ingenuity Pro CT5000 Ingenuity… recall
  FDA August 5, 2026 · Philips Medical Systems · Class II
• IQon Spectral CT IQon Spectral CT Upgrades recall
  FDA August 5, 2026 · Philips Medical Systems · Class II
• Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64… recall
  FDA August 5, 2026 · Philips Medical Systems · Class II
• Mellish Island Super Skin recall
  FDA August 5, 2026 · Mellish Island Corp · Class II