FDA Device recall Z-2738-2026
Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010
- FDA Device
- Class II
- ongoing
- Published 2026-07-22
On 2026-07-22 the FDA classified a Class II recall of Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010 by Medtronic Perfusion Systems, citing medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2738-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-05-25 |
| Published | 2026-07-22 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Medtronic Perfusion Systems |
| Distribution | US |
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.
Identifiers
| code_info | MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2738-2026%22
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