Medtronic DLP Single Stage Venous Cannulae with right angle metal tip — Class II medical device recall Z-3128-2024
Ongoing recall by Medtronic Perfusion Systems, reported 2024-09-18, distributed nationwide. During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed int
| Recall number | Z-3128-2024 |
|---|---|
| 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 | 2024-07-09 |
| Classified | 2024-09-12 |
| Reported by FDA | 2024-09-18 |
| Distributed | Nationwide (US) |
| Countries outside the US | CH, GB, GR, IE, IT, SA, VN |
| Quantity | 290 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 20613994879329 |
| Lot numbers | 2023090954, 202312C065 |
| Model numbers | 67312 |
Product
Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
Reason for recall
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).
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-3128-2024. 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.