Medical devices recalls – page 11

• 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
• OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites recall
  FDA July 8, 2026 · Bd Switzerland Sarl · Class II
• Covidien Shiley Disposable Decannulation Plug recall
  FDA July 8, 2026 · Covidien, LP · Class II
• Zeiss Intrabeam Spherical Applicator 1.5 cm recall
  FDA July 8, 2026 · Carl Zeiss Meditec AG · Class II
• ARTIS icono ceiling recall
  FDA July 8, 2026 · Siemens Medical Solutions USA, Inc · Class II
• RayCare 2024A SP4. Oncology Information Systems recall
  FDA July 8, 2026 · Raysearch Laboratories Ab · Class II
• RayCare 2024A SP1. Oncology Information Systems recall
  FDA July 8, 2026 · Raysearch Laboratories Ab · Class II
• Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model recall
  FDA July 8, 2026 · Medela Inc · Class II
• Cyberknife Treatment Deliver System equipped with the Xchange Robotic… recall
  FDA July 8, 2026 · Accuray Incorporated · Class II
• ARTIS icono floor recall
  FDA July 8, 2026 · Siemens Medical Solutions USA, Inc · Class II
• ARTIS icono ceiling recall
  FDA July 8, 2026 · Siemens Medical Solutions USA, Inc · Class II
• ARTIS icono biplane recall
  FDA July 8, 2026 · Siemens Medical Solutions USA, Inc · Class II
• Cyberknife Treatment Deliver System equipped with the Xchange Robotic… recall
  FDA July 8, 2026 · Accuray Incorporated · Class II
• Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton)… recall
  FDA July 8, 2026 · Teleflex LLC · Class II
• Adapter for Head Positioning, Model recall
  FDA July 8, 2026 · Baxter Healthcare Corporation · Class II
• CRE Wireguided 18-20mm 240cm recall
  FDA July 8, 2026 · Boston Scientific Corporation · Class II
• CRE Wireguided 15-18mm 240cm recall
  FDA July 8, 2026 · Boston Scientific Corporation · Class II
• CRE Wireguided 12-15mm 240cm recall
  FDA July 8, 2026 · Boston Scientific Corporation · Class II
• CRE Wireguided 10-12mm 240cm recall
  FDA July 8, 2026 · Boston Scientific Corporation · Class II
• CRE Wireguided 8-10mm 240cm recall
  FDA July 8, 2026 · Boston Scientific Corporation · Class II
• CRE Wireguided 6-8mm 240cm recall
  FDA July 8, 2026 · Boston Scientific Corporation · Class II
• CRE Pro Wireguided 18-20mm 240cm recall
  FDA July 8, 2026 · Boston Scientific Corporation · Class II
• CRE Pro Wireguided 15-18mm 240cm recall
  FDA July 8, 2026 · Boston Scientific Corporation · Class II
• CRE Pro Wireguided 12-15mm 240cm recall
  FDA July 8, 2026 · Boston Scientific Corporation · Class II
• CRE Pro Wireguided 10-12mm 240cm recall
  FDA July 8, 2026 · Boston Scientific Corporation · Class II
• CRE Pro Wireguided 8-10mm 240cm recall
  FDA July 8, 2026 · Boston Scientific Corporation · Class II
• CRE Pro Wireguided 6-8mm 240cm recall
  FDA July 8, 2026 · Boston Scientific Corporation · Class II
• IntelliCuff, Portable automatic cuff pressure controller recall
  FDA July 8, 2026 · Hamilton Medical AG · Class II
• Medtronic Harmony Delivery Catheter System recall
  FDA July 8, 2026 · Medtronic Heart Valves Division · Class I
• GC Agar Base (150mm) 10/PK R04030 recall
  FDA July 8, 2026 · Remel, Inc · Class II
• A M S, ALIGNED MEDICAL SOLUTIONS, Dr recall
  FDA July 8, 2026 · Windstone Medical Packaging, Inc. · Class I
• A M S, ALIGNED MEDICAL SOLUTIONS, Preop Kit-NS, Pack Number AMS18227… recall
  FDA July 8, 2026 · Windstone Medical Packaging, Inc. · Class I
• A M S, ALIGNED MEDICAL SOLUTIONS, Thyroid FNA Pack-RX… recall
  FDA July 8, 2026 · Windstone Medical Packaging, Inc. · Class I
• A M S, ALIGNED MEDICAL SOLUTIONS, DSAEK Pack-RX, Pack Number AMS12394B… recall
  FDA July 8, 2026 · Windstone Medical Packaging, Inc. · Class I
• Short Monobloc Stem Broaches, Size recall
  FDA July 8, 2026 · Medacta Usa Inc · Class II
• Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the… recall
  FDA July 8, 2026 · Depuy (Ireland) · Class II
• Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Housing Components with… recall
  FDA July 8, 2026 · Depuy (Ireland) · Class II
• Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no recall
  FDA July 8, 2026 · Medline Industries, LP · Class I
• SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code:… recall
  FDA July 8, 2026 · Mentor Texas, LP. · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters CV… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters KIT… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters CENTRAL… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II