FDAFDA · Food and drugs·Recall number Z-2738-2026
Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
Published July 22, 2026 · Recall initiated: May 25, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Medtronic Perfusion Systems
- Distributor
- Worldwide - US Nationwide distribution in the states of MD, CA, MI, WA, PA, NC, FL, AR.
- Lot
- MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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