Medtronic DLP One-Piece Pediatric Arterial Cannula recall (Medtronic Perfusion Systems)
Medical deviceClass IIOngoing
Summary: Medtronic Perfusion Systems is recalling 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.
What is being recalled
Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
Why
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
Worldwide - US Nationwide distribution in the states of MD, CA, MI, WA, PA, NC, FL, AR. (states named: Arkansas, California, Florida, Maryland, Michigan, North Carolina, Pennsylvania, Washington)
How to tell if yours is affected
MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-2738-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | May 25, 2026 |
| Reported | July 22, 2026 |
| Company | Medtronic Perfusion Systems |
| Company location | Brooklyn Park, MN, United States |
| Initiated by | Voluntary: Firm initiated |
More recalls from Medtronic Perfusion Systems · all medical device recalls · recalls from May 2026