Class II medical devices recalls – page 9

• Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115 recall
  FDA July 22, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP One-Piece Pediatric Arterial Cannula… recall
  FDA July 22, 2026 · Medtronic Perfusion Systems · 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
• Papablic Replacement Brush Heads recall
  FDA July 22, 2026 · Papablic Inc · Class II
• Papablic Replacement Brush Heads recall
  FDA July 22, 2026 · Papablic Inc · 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
• Optima XR240amx, Mobile Digital Radiographic System recall
  FDA July 22, 2026 · GE Medical Systems, LLC · Class II
• Optima XR220amx, Mobile Digital-Ready Radiographic System recall
  FDA July 22, 2026 · GE Medical Systems, LLC · Class II
• Optima XR200amx, Mobile Digital-Ready Radiographic System recall
  FDA July 22, 2026 · GE Medical Systems, LLC · Class II
• Rapid Refill Continuous Injection System, UPN M00566001 recall
  FDA July 22, 2026 · Boston Scientific Corporation · Class II
• ICU Medical Plum Solo Precision IV Pump, v1.0.3, Item Number 400010401 recall
  FDA July 22, 2026 · ICU Medical, Inc. · Class II
• ICU Medical Plum Duo Infusion Pump, v1.2.3: 1) Item Number 400020401 and… recall
  FDA July 22, 2026 · ICU Medical, 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
• Olympus Glass Body for 194 Ellik Evacuator recall
  FDA July 22, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Ellik Evacuator Includes Glass Body… recall
  FDA July 22, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Toomey Evacuator 50cc with Adaptor recall
  FDA July 22, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Toomey Evacuator 30cc with Adaptor recall
  FDA July 22, 2026 · Olympus Corporation of the Americas · Class II
• Versius Surgical System US Product Name: Vesius Surgeon Console US Model recall
  FDA July 15, 2026 · Cmr Surgical Limited · Class II
• TMINI Femur Tracking Array recall
  FDA July 15, 2026 · Think Surgical, Inc. · Class II
• VITEK 2 AST-N447 TEST KIT Product reference 424620 recall
  FDA July 15, 2026 · Biomerieux Inc · Class II
• OmniTract Surgical Retractor System, which includes 633 of the firm s… recall
  FDA July 15, 2026 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• GSP Neonatal GALT Kit recall
  FDA July 15, 2026 · Wallac Oy · 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
• Atellica CH Enzymatic Hemoglobin A1c (A1c_E) recall
  FDA July 15, 2026 · Siemens Healthcare Diagnostics, Inc. · Class II
• 5008X Blood Tubing Set, 24 units per case recall
  FDA July 15, 2026 · Fresenius Medical Care Holdings, Inc. · Class II
• EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model recall
  FDA July 15, 2026 · Encore Medical, LP · Class II
• EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model recall
  FDA July 15, 2026 · Encore Medical, LP · Class II
• KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033 recall
  FDA July 15, 2026 · Klowen Braces · Class II
• MiniMed 780G Insulin Pump recall
  FDA July 15, 2026 · Medtronic MiniMed, Inc. · Class II
• Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569 recall
  FDA July 15, 2026 · Medline Industries, LP · Class II
• Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569D recall
  FDA July 15, 2026 · Medline Industries, LP · Class II
• Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF… recall
  FDA July 15, 2026 · Medline Industries, LP · Class II
• Intracept Access Instruments, Description recall
  FDA July 15, 2026 · Boston Scientific Neuromodulation Corporation · Class II
• Aquacel Ag Surgical SP recall
  FDA July 15, 2026 · ConvaTec, Inc · Class II
• Olympus Single Use Distal Cover recall
  FDA July 15, 2026 · Olympus Corporation of the Americas · Class II
• Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems… recall
  FDA July 8, 2026 · Zimmer Surgical Inc · Class II
• Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems… recall
  FDA July 8, 2026 · Zimmer Surgical Inc · 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
• Solar GI System (Water Perfusion) recall
  FDA July 8, 2026 · Laborie Medical Technologies Corp · 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
• CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II