Medtronic Perfusion Systems recalls
21 recalls.
- EOPA 3D Arterial Cannula 22FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported August 5, 2026 · Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel... - EOPA 3D Arterial Cannula DIL TIP 22FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported August 5, 2026 · Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel... - EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported August 5, 2026 · Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel... - EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported August 5, 2026 · Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel... - EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported August 5, 2026 · Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel... - EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported August 5, 2026 · Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel... - Medtronic Bio-Medicus Adult Cannula Kit recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 22, 2026 · Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood. - Medtronic DLP One-Piece Pediatric Arterial Cannula recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 22, 2026 · Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood. - Octopus 4 Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Octopus Evolution AS Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Octopus Evolution Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Octopus Nuvo Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported March 4, 2026 · During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the...