Recalls distributed in Minnesota – page 3

• ERBECRYO 2 Cryosurgical Unit Model recall
  FDA August 19, 2026 · Erbe USA Inc · Class II
• BIOFIRE Respiratory Panel 2.1 (RP2.1) recall
  FDA August 19, 2026 · BioFire Diagnostics, LLC · Class II
• OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source… recall
  FDA August 19, 2026 · OBP Medical Corporation · Class II
• Boston Scientific Enhance Transcarotid/Peripheral Access Kit recall
  FDA August 19, 2026 · Galt Medical Corporation · Class II
• Xhibit Product Name: Xhibit Central Station Model recall
  FDA August 19, 2026 · Spacelabs Healthcare, Inc. · Class II
• navify Digital Pathology (on-prem) v2.5, Material Number 10092343001… recall
  FDA August 19, 2026 · Ventana Medical Systems, Inc. · Class II
• BOBBY Balloon Guide Catheter recall
  FDA August 19, 2026 · Microvention Inc. · Class II
• Aquafaba Powder, Vegan Replacement, NET WT… recall
  FDA August 19, 2026 · 529 Commerce, LLC · Class I
• 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
• FilmArray NGDS Warrior Panel recall
  FDA August 12, 2026 · Biofire Defense · 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
• Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree… recall
  FDA August 12, 2026 · PT Organics Limited · 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
• MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android) recall
  FDA July 29, 2026 · Medtronic MiniMed, Inc. · Class II
• Boston Scientific TheraSphere 360 Y-90 Management Platform… recall
  FDA July 29, 2026 · Boston Scientific Corporation · Class II
• Penumbra System RED 68 Reperfusion Catheter recall
  FDA July 29, 2026 · Penumbra, Inc. · Class II
• 3mensio Workstation (Vascular Fenestrated) software recall
  FDA July 29, 2026 · PIE Medical Imaging B.V. · Class II
• Power F2 Powered Fastening System, Product No recall
  FDA July 29, 2026 · Ferno-Washington Inc · Class II
• da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13… recall
  FDA July 22, 2026 · Intuitive Surgical, Inc. · Class II
• functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT… recall
  FDA July 22, 2026 · Nutricia North America · Class II
• functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT… recall
  FDA July 22, 2026 · Nutricia North America · Class II
• TMINI Femur Tracking Array recall
  FDA July 15, 2026 · Think Surgical, Inc. · Class II