Medtronic DLP Vessel Cannula — Class II medical device recall Z-1316-2024
Ongoing recall by Medtronic Perfusion Systems, reported 2024-03-27, distributed in GA. Medtronic is writing to inform you of incorrect labeling for three manufactured lots of the DLP Vessel Cannula
| Recall number | Z-1316-2024 |
|---|---|
| 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 | 2024-02-07 |
| Classified | 2024-03-19 |
| Reported by FDA | 2024-03-27 |
| Distributed | GA |
| Countries outside the US | BR, CA, DE, GB, IE, IN, IT, MY, ZA |
| Quantity | 4,343 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 20613994646211 |
| Lot numbers | 2023020889, 2023020890, 202305C126 |
| Model numbers | 30000 |
Product
Medtronic DLP Vessel Cannula, Model Number REF 30000
Reason for recall
Medtronic is writing to inform you of incorrect labeling for three manufactured lots of the DLP Vessel Cannulae for the model and lot numbers listed above.
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-1316-2024. 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.