Medtronic Perfusion Systems recalls

All Medtronic Perfusion Systems recalls we track from FDA, CPSC and NHTSA data. Categories: medical devices (32).

32 recalls published between November 13, 2024 and August 5, 2026. Most common issues: sterility (10), laceration (6), mislabeling (3), foreign material (2). 4 were FDA Class I, the most serious level.

• EOPA 3D Arterial Cannula 22FR, intended for use with cardiopulmonary… recall
  FDA August 5, 2026 · Medtronic Perfusion Systems · Class II
• EOPA 3D Arterial Cannula DIL TIP 22FR, intended for use with… recall
  FDA August 5, 2026 · Medtronic Perfusion Systems · Class II
• EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR… recall
  FDA August 5, 2026 · Medtronic Perfusion Systems · Class II
• EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR… recall
  FDA August 5, 2026 · Medtronic Perfusion Systems · Class II
• EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR… recall
  FDA August 5, 2026 · Medtronic Perfusion Systems · Class II
• EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR… recall
  FDA August 5, 2026 · Medtronic Perfusion Systems · Class II
• 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
• Octopus 4 Tissue Stabilizer, Model 29400 recall
  FDA July 1, 2026 · Medtronic Perfusion Systems · Class II
• Octopus Evolution AS Tissue Stabilizer, Model TS2500 recall
  FDA July 1, 2026 · Medtronic Perfusion Systems · Class II
• Octopus Evolution Tissue Stabilizer, Model TS2000 recall
  FDA July 1, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR… recall
  FDA May 27, 2026 · Medtronic Perfusion Systems · Class II
• Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system… recall
  FDA March 4, 2026 · Medtronic Perfusion Systems · Class II
• Medtronic HR-ACT (High Range Activated Clotting Time Cartridges) recall
  FDA November 26, 2025 · Medtronic Perfusion Systems · Class II
• MC3 VitalFlow Console recall
  FDA November 26, 2025 · Medtronic Perfusion Systems · Class II
• Affinity NT Oxygenator, Oxygenator with Balance Biosurface and Uncoated… recall
  FDA November 19, 2025 · Medtronic Perfusion Systems · Class II
• DLP Left Heart Vent Catheter Malleable body and vented connector… recall
  FDA September 10, 2025 · Medtronic Perfusion Systems · Class I
• DLP Left Heart Vent Catheter Malleable body and vented connector… recall
  FDA September 10, 2025 · Medtronic Perfusion Systems · Class I
• DLP Left Heart Vent Catheter Malleable body and vented connector… recall
  FDA September 10, 2025 · Medtronic Perfusion Systems · Class I
• Aortic Root Cannula: 1. DLP Aortic Root Cannula A… recall
  FDA March 19, 2025 · Medtronic Perfusion Systems · Class I
• Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr) recall
  FDA January 29, 2025 · Medtronic Perfusion Systems · Class II
• EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr) recall
  FDA January 29, 2025 · Medtronic Perfusion Systems · Class II
• DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and… recall
  FDA January 29, 2025 · Medtronic Perfusion Systems · Class II
• Medtronic DLP Aortic Root Cannula with Flow-Guard recall
  FDA November 13, 2024 · Medtronic Perfusion Systems · Class II