FDA
Food and Drug Administration · Recall Z-2738-2026 · May 25, 2026Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
Medtronic Perfusion Systems
The hazard
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model MATNR A7630009466801/UDI/DI 20763000946689Model Lot Numbers: 0231650870Model C232227220UPC 20763000946689Would you have heard about this one?
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Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.