FDA Device recall Z-3128-2024
Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
- FDA Device
- Class II
- ongoing
- Published 2024-09-18
On 2024-09-18 the FDA classified a Class II recall of Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312 by Medtronic Perfusion Systems, citing during manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3128-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-07-09 |
| Published | 2024-09-18 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medtronic Perfusion Systems |
| Distribution | US |
Product
Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
Reason
During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312).
Identifiers
| code_info | GTIN 20613994879329, Lot Numbers: 2023090954, 202312C065 |
|---|
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-3128-2024%22
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