Medtronic Perfusion Systems recalls

20 recent recalls on record for Medtronic Perfusion Systems in connected official government data as of September 7, 2026 at 6:00 AM UTC.

Models with recalls

EOPA 3D Arterial Cannula 22FR (1)EOPA 3D Arterial Cannula DIL TIP 22FR (1)EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR (2)EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR (2)Medtronic Bio-Medicus Adult Cannula Kit (1)Medtronic DLP One-Piece Pediatric Arterial Cannula (1)Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR (7)Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR (2)Octopus 4 Tissue Stabilizer (1)Octopus Evolution AS Tissue Stabilizer (1)Octopus Evolution Tissue Stabilizer (1)

All Medtronic Perfusion Systems recalls

FDA Class II · Medical device · August 5, 2026

EOPA 3D Arterial Cannula 22FR recall — Medtronic Perfusion Systems

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…

Official ID Z-2811-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

EOPA 3D Arterial Cannula DIL TIP 22FR recall — Medtronic Perfusion Systems

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…

Official ID Z-2810-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR recall — Medtronic Perfusion Systems

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…

Official ID Z-2809-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR recall — Medtronic Perfusion Systems

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…

Official ID Z-2808-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR recall — Medtronic Perfusion Systems

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…

Official ID Z-2807-2026 · Official record ↗

FDA Class II · Medical device · August 5, 2026

EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR recall — Medtronic Perfusion Systems

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforati…

Official ID Z-2806-2026 · Official record ↗

FDA Class II · Medical device · July 22, 2026

Medtronic Bio-Medicus Adult Cannula Kit recall — Medtronic Perfusion Systems

Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.

Official ID Z-2739-2026 · Official record ↗

FDA Class II · Medical device · July 22, 2026

Medtronic DLP One-Piece Pediatric Arterial Cannula recall — Medtronic Perfusion Systems

Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.

Official ID Z-2738-2026 · Official record ↗

FDA Class II · Medical device · July 1, 2026

Octopus 4 Tissue Stabilizer recall — Medtronic Perfusion Systems

During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the can…

Official ID Z-2577-2026 · Official record ↗

FDA Class II · Medical device · July 1, 2026

Octopus Evolution AS Tissue Stabilizer recall — Medtronic Perfusion Systems

During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the can…

Official ID Z-2576-2026 · Official record ↗

FDA Class II · Medical device · July 1, 2026

Octopus Evolution Tissue Stabilizer recall — Medtronic Perfusion Systems

During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the can…

Official ID Z-2575-2026 · Official record ↗

FDA Class II · Medical device · May 27, 2026