FDA Device recall Z-1316-2024
Medtronic DLP Vessel Cannula, Model Number REF 30000
- FDA Device
- Class II
- ongoing
- Published 2024-03-27
On 2024-03-27 the FDA classified a Class II recall of Medtronic DLP Vessel Cannula, Model Number REF 30000 by Medtronic Perfusion Systems, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1316-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-02-07 |
| Published | 2024-03-27 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medtronic Perfusion Systems |
| Distribution | GA |
Product
Medtronic DLP Vessel Cannula, Model Number REF 30000
Reason
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.
Identifiers
| code_info | UDI/DI 20613994646211, Lot Numbers: 2023020890, 202305C126, 2023020889 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1316-2024%22
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