Medtronic Perfusion Systems recalls Medtronic DLP One-Piece Pediatric Arterial Cannula
- Recalling company
- Medtronic Perfusion Systems
- Product
- Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
- Reason
- Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- May 25, 2026
- Reported
- Jul 22, 2026
- Distribution
- Worldwide - US Nationwide distribution in the states of MD, CA, MI, WA, PA, NC, FL, AR.
- Status
- Ongoing
- Lot / codes
- MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220
- Company location
- Brooklyn Park, MN
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2738-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2738-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.