FDA Device recall Z-2739-2026
Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115
- FDA Device
- Class II
- ongoing
- Published 2026-07-22
On 2026-07-22 the FDA classified a Class II recall of Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115 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-2739-2026 |
| 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 Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115; Cardiopulmonary bypass vascular cannula
Reason
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
Identifiers
| code_info | MATNR 00763000116019/UDI/DI 00643169769076, Lot Number: 230257001 |
|---|
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-2739-2026%22
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