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FDA
Food and Drug Administration · Recall Z-2807-2026 · Jun 24, 2026

EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77522

Medtronic Perfusion Systems

The hazard

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 dysfunction. FDA Class II recall.

The remedy

Follow FDA guidance

About this recall

EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77522

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

Model UDI-DI: 00199150023288Model Lot Numbers: 0233286436Model UDI-DI: 20199150023282UPC 00199150023288UPC 20199150023282

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.