Medical devices recalls – page 32

• Medline Convenience Kits: 1) OR ARTERIOGRAM, Model Number: CDS985094F recall
  FDA February 25, 2026 · Medline Industries, LP · Class II
• Medline Convenience Kits: 1) ENDO KIT W/SYRINGE, Model Number: DYKE1743 recall
  FDA February 25, 2026 · Medline Industries, LP · Class II
• Medline Convenience Kits: 1) BASIC NERVE BLOCK TRAY W/LINEN… recall
  FDA February 25, 2026 · Medline Industries, LP · Class II
• Medline Convenience Kits: 1) SCC RF PAIN MGMT, Model Number: DYNJ56436A recall
  FDA February 25, 2026 · Medline Industries, LP · Class II
• Medline Convenience Kits: 1) KIT STC TRACHEOSTOMY, Model Number: DYKMBNDL55 recall
  FDA February 25, 2026 · Medline Industries, LP · Class II
• Medline Convenience Kits: 1) ANCILLARY PACK-LF, Model Number: DYNJ0185290G recall
  FDA February 25, 2026 · Medline Industries, LP · Class II
• MONARCH Platform, Bronchoscopy recall
  FDA February 25, 2026 · Auris Health, Inc · Class II
• Olympus Thunderbeat 5 mm, 10 cm, Inline Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5 mm, 20 cm, Inline Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5 mm, 35 cm, Inline Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5 mm, 45 cm Inline Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5mm, 35 cm, Pistol Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5 mm, 45 cm, Pistol Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat 5 mm, 35 cm, Front-Actuated Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5 mm, 45 cm Front-Actuated Grip recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip Type S recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat, 5 mm, 35 cm, Front-Actuated Grip Type S recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Olympus Thunderbeat 5 mm, 45 cm, Front-Actuated Grip Type S recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class II
• Medica Capillary Tubes recall
  FDA February 25, 2026 · Medica Corporation · Class II
• Estrone RIA recall
  FDA February 25, 2026 · Immunotech A.S. · Class II
• Spectrum IQ Product Name: Infusion Pump Model recall
  FDA February 25, 2026 · Baxter Healthcare Corporation · Class II
• Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue… recall
  FDA February 25, 2026 · Bard Peripheral Vascular Inc · Class II
• Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN… recall
  FDA February 25, 2026 · Medline Industries, LP · Class II
• Private Label CVS. Model Number: CVS405406… recall
  FDA February 25, 2026 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY… recall
  FDA February 25, 2026 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• MediHoney Gel with Active Leptospermum Honey recall
  FDA February 25, 2026 · Integra LifeSciences Corp. (NeuroSciences) · Class II
• Teslatome Bipolar Sphincterotomes recall
  FDA February 25, 2026 · Wilson-Cook Medical Inc. · Class II
• Olympus High Flow Insufflation Unit recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class I
• Olympus High Flow Insufflation Unit recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class I
• Olympus High Flow Insufflation Unit recall
  FDA February 25, 2026 · Olympus Corporation of the Americas · Class I
• Barco MNA with the HexaVue IP Integration System, Model recall
  FDA February 18, 2026 · Steris Corporation · Class II
• Surepulse VS Cap Extra Large recall
  FDA February 18, 2026 · Surepulse Medical Ltd · Class III
• Surepulse VS Cap Large recall
  FDA February 18, 2026 · Surepulse Medical Ltd · Class III
• Surepulse VS Cap Medium recall
  FDA February 18, 2026 · Surepulse Medical Ltd · Class III
• Surepulse VS Cap Small recall
  FDA February 18, 2026 · Surepulse Medical Ltd · Class III
• Surepulse VS Cap Extra Small recall
  FDA February 18, 2026 · Surepulse Medical Ltd · Class III
• da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000… recall
  FDA February 18, 2026 · Intuitive Surgical, Inc. · Class II
• Azurion 5 M20 System Model Numbers: (1)722228, (2)722232… recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 5 M12 System Model Numbers: (1)722227, (2)722231 recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234… recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233 recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 B20 System Model Numbers: (1)722068, (2)722226, (3)722236 recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235 recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230… recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 3 M12 System Model Numbers: (1) 722063, (2) 722221, (3) 722229 recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm recall
  FDA February 18, 2026 · Alphatec Spine, Inc. · Class II
• ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm recall
  FDA February 18, 2026 · Alphatec Spine, Inc. · Class II
• Laerdal Compact Suction Unit 4 RTCA version (LCSU 4 RTCA) 1) LCSU 4… recall
  FDA February 18, 2026 · Laerdal Medical Corporation · Class II
• Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system… recall
  FDA February 18, 2026 · Elekta, Inc. · Class II
• Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system… recall
  FDA February 18, 2026 · Elekta, Inc. · Class II
• Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01 recall
  FDA February 18, 2026 · AVID Medical, Inc. · Class II
• WB Impression Post Closed Tray incl recall
  FDA February 18, 2026 · Straumann USA LLC · Class III
• Medline medical convenience kits packaged as: MERCY CIRCUMCISION TRAY… recall
  FDA February 18, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits packaged as: STERILE RESUTURE PACK… recall
  FDA February 18, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits packaged as: ) LVAD DRESSING CHANGE TRAY… recall
  FDA February 18, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits packaged as: BLOOD CULTURE KIT NS… recall
  FDA February 18, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY… recall
  FDA February 18, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits packaged as: 1) POWERGLIDE DRESSING… recall
  FDA February 18, 2026 · Medline Industries, LP · Class II
• 1) UNIVERSAL KIT, Kit SKU DT22010B recall
  FDA February 18, 2026 · Medline Industries, LP · Class II