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RecallsAboutBlog

Medtronic Perfusion Systems

Medtronic Perfusion Systems: 5 recalls listed since February 2026 across FDA.

By year

  • 20265

By agency

  • FDA5

By category

  • Medical Device5

All recalls (5)

Medtronic EOPA Arterial Cannulas

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass.

Moderate risk, FDA, , Device defect

Medtronic DLP and Bio-Medicus Cannulas

The Medtronic DLP One-Piece Pediatric Arterial Cannula may contain loose foreign material with trace blood.

Moderate risk, FDA, , Foreign object

Octopus 4, Evolution, and Evolution AS Tissue Stabilizer

The Octopus Evolution Tissue Stabilizer has an assembly issue where tubing was incorrectly positioned.

Moderate risk, FDA, , Manufacturing problem

Medtronic Gundry and DLP Retrograde Cannulas

Medtronic retrograde cannulas may have a sterile barrier breach.

Moderate risk, FDA, , Sterility problem

Medtronic Octopus Nuvo Tissue Stabilizer

The Octopus Nuvo Tissue Stabilizer has tubing incorrectly positioned, which may cause assembly issues.

Moderate risk, FDA, , Manufacturing problem
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