Recalls distributed in Utah – page 2

• ERBECRYO 2 Cryosurgical Unit Model recall
  FDA August 19, 2026 · Erbe USA Inc · Class II
• OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source… recall
  FDA August 19, 2026 · OBP Medical Corporation · Class II
• GM Helix Implant, Endosseous Dental Implant Article No recall
  FDA August 19, 2026 · Straumann USA LLC · Class II
• navify Digital Pathology (on-prem) v2.5, Material Number 10092343001… recall
  FDA August 19, 2026 · Ventana Medical Systems, Inc. · Class II
• Aquafaba Powder, Vegan Replacement, NET WT… recall
  FDA August 19, 2026 · 529 Commerce, LLC · Class I
• FilmArray NGDS Warrior Panel recall
  FDA August 12, 2026 · Biofire Defense · 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
• Vanderhall North America Recalls Brawley GTS Electric Recreational Off Highway Vehicles (ROVs) Due to Risk of Serious Injury or Death from…
  CPSC August 6, 2026 · Vanderhall North America
• 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
• MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android) recall
  FDA July 29, 2026 · Medtronic MiniMed, Inc. · Class II
• SnapshotGLO Wound Imaging Device, Model KB100, KB100AA recall
  FDA July 29, 2026 · Kent Imaging, 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
• Ventriculostomy Kit recall
  FDA July 29, 2026 · Medtronic Neurosurgery · Class II
• SeaSpine Polyaxial Head recall
  FDA July 29, 2026 · Seaspine Orthopedics Corporation · Class II
• Power F2 Powered Fastening System, Product No recall
  FDA July 29, 2026 · Ferno-Washington Inc · Class II
• Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE… recall
  FDA July 22, 2026 · Medline Industries, LP · Class II
• Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE… recall
  FDA July 22, 2026 · Medline Industries, LP · Class II
• Orthofix MINIRAIL, ARTICULATED, FIXATOR, VERTICAL AXIS recall
  FDA July 22, 2026 · Orthofix U.S. LLC · Class II
• Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS recall
  FDA July 22, 2026 · Orthofix U.S. LLC · Class II
• Orthofix MINIRAIL, SHORT, LENGTHENER recall
  FDA July 22, 2026 · Orthofix U.S. LLC · Class II
• Orthofix MINIRAIL, STANDARD LENGTHENER Model recall
  FDA July 22, 2026 · Orthofix U.S. LLC · 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
• Geneva Product Name: Brachytherapy Applicator Product Description: The… recall
  FDA July 15, 2026 · Elekta, Inc. · Class II
• Brachytherapy Applicator Product Name: Advanced Gynecological Applicator… recall
  FDA July 15, 2026 · Elekta, Inc. · Class II
• Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote… recall
  FDA July 15, 2026 · Elekta, Inc. · Class II
• Intracept Access Instruments, Description recall
  FDA July 15, 2026 · Boston Scientific Neuromodulation Corporation · Class II
• Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough… recall
  FDA July 15, 2026 · Bear Stewart Co · Class II
• GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component recall
  FDA July 8, 2026 · W L Gore & Associates, Inc. · Class II
• Radius VSM Disposable NIBP Cuff recall
  FDA July 8, 2026 · Masimo Corporation · Class II
• Radius VSM ECG pre-connected Set recall
  FDA July 8, 2026 · Masimo Corporation · Class II
• 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II