Medtronic Bio-Medicus Adult Cannula Kit — Class II medical device recall Z-2739-2026
Ongoing recall by Medtronic Perfusion Systems, reported 2026-07-22, distributed nationwide. Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
| Recall number | Z-2739-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Perfusion Systems, Brooklyn Park, MN, United States |
| Recall initiated | 2026-05-25 |
| Classified | 2026-07-15 |
| Reported by FDA | 2026-07-22 |
| Distributed | Nationwide (US) |
| Reason classes | foreign material |
| UPC / GTIN / UDI-DI | 00643169769076, 00763000116019 |
| Lot numbers | 230257001 |
Product
Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115; Cardiopulmonary bypass vascular cannula
Reason for recall
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2739-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.