Class IIOngoingZ-3146-2026
Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit (PIK)
The packaging may not consistently maintain sterile barrier integrity.
Maquet Cardiopulmonary…Sep 23, 2026
Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–12 of 20 recalls
Class IIOngoingZ-3145-2026
Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit (PIK)
The packaging may not consistently maintain sterile barrier integrity.
Maquet Cardiopulmonary…Sep 23, 2026
Class IIOngoingZ-3144-2026
Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit (PIK)
The packaging may not consistently maintain sterile barrier integrity.
Maquet Cardiopulmonary…Sep 23, 2026
Class IIOngoingZ-2811-2026
Medtronic Perfusion Systems recalls EOPA 3D Arterial Cannula 22FR
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dys…
Medtronic Perfusion Sy…MNAug 5, 2026
Class IIOngoingZ-2810-2026
Medtronic Perfusion Systems recalls EOPA 3D Arterial Cannula DIL TIP 22FR
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dys…
Medtronic Perfusion Sy…MNAug 5, 2026
Class IIOngoingZ-2809-2026
Medtronic Perfusion Systems recalls EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dys…
Medtronic Perfusion Sy…MNAug 5, 2026
Class IIOngoingZ-2808-2026
Medtronic Perfusion Systems recalls EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dys…
Medtronic Perfusion Sy…MNAug 5, 2026
Class IIOngoingZ-2807-2026
Medtronic Perfusion Systems recalls EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dys…
Medtronic Perfusion Sy…MNAug 5, 2026
Class IIOngoingZ-2806-2026
Medtronic Perfusion Systems recalls EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dys…
Medtronic Perfusion Sy…MNAug 5, 2026
Class IIOngoingZ-2739-2026
Medtronic Perfusion Systems recalls Medtronic Bio-Medicus Adult Cannula Kit
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
Medtronic Perfusion Sy…MNJul 22, 2026
Class IIOngoingZ-2738-2026
Medtronic Perfusion Systems recalls Medtronic DLP One-Piece Pediatric Arterial Cannula
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
Medtronic Perfusion Sy…MNJul 22, 2026
Class IIOngoingZ-2222-2026
Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR
Certain lots of product have the potential for a sterile barrier breach.
Medtronic Perfusion Sy…MNMay 27, 2026