Medtronic Perfusion Systems: Medical Device Recalls in 2025

According to to data from the FDA, there were 10 medical device recalls made by Medtronic Perfusion Systems in 2025. See the details of the recalls below.

You can see similar recalls for other firms.

• DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12110 LV VENT 10FR, Model Number 12110
• DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12115 LV VENT 15FR, Model Number 12115
• DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12113 LV VENT 13FR, Model Number 12113
• Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA 11012 AR FLOWGUARD 12GA, model no 11012 B. CANNULA 11014 AR FLOWGUARD 14GA, model no. 11014 2. MiAR Cannula: A. CANNULA 11012L AR FLOWGUARD LONG 12GA, model no 11012L B. CANNULA 11014L AR FLOWGUARD 14FR LONG, model no. 11014L 3. DLP Aortic Root Cannula with Vent Line A. CANNULA 21012 AR VENT FLOW 12GA, model no. 21012 B. CANNULA 21014 AR VENT FLOW 14GA, model no. 21014
• EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)
• DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr)
• Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
• Medtronic HR-ACT (High Range Activated Clotting Time Cartridges), REF 402-03
• MC3 VitalFlow Console, REF 58100; Blood pump of ecmo
• Affinity NT Oxygenator, Oxygenator with Balance Biosurface and Uncoated Cardiotomy/Venous Reservoir, Product Number 541B