Class IOngoingZ-2482-2025
Medtronic Perfusion Systems recalls DLP Left Heart Vent Catheter Malleable body and vented connector
The catheters may not retain their shape.
Medtronic Perfusion Sy…MNSep 10, 2025
Medtronic Perfusion Systems recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 25–31 of 31 recalls
Class IOngoingZ-2481-2025
Medtronic Perfusion Systems recalls DLP Left Heart Vent Catheter Malleable body and vented connector
The catheters may not retain their shape.
Medtronic Perfusion Sy…MNSep 10, 2025
Class IOngoingZ-2480-2025
Medtronic Perfusion Systems recalls DLP Left Heart Vent Catheter Malleable body and vented connector
The catheters may not retain their shape.
Medtronic Perfusion Sy…MNSep 10, 2025
Class IOngoingZ-1306-2025
Medtronic Perfusion Systems recalls Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA 11012 AR FLOWGUARD 12GA
Unexpected loose material in the male luer used in the aortic root cannula has been identified. Potential harms when identified prior to use - procedure delay.…
Medtronic Perfusion Sy…MNMar 19, 2025
Class IIOngoingZ-0986-2025
Medtronic Perfusion Systems recalls Select Series Angled Tip Arterial Cannula
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Medtronic Perfusion Sy…MNJan 29, 2025
Class IIOngoingZ-0985-2025
Medtronic Perfusion Systems recalls EOPA Arterial Cannula
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Medtronic Perfusion Sy…MNJan 29, 2025
Class IIOngoingZ-0984-2025
Medtronic Perfusion Systems recalls DLP Pediatric One-Piece Arterial Cannulae
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Medtronic Perfusion Sy…MNJan 29, 2025