Medtronic REF 46915 Duet External Drainage and Monitoring system — Class II medical device recall Z-2412-2023
Ongoing recall by Medtronic Neurosurgery, reported 2023-08-23, distributed nationwide. Product labeling contains incorrect expiration date
| Recall number | Z-2412-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Neurosurgery, Irvine, CA, United States |
| Recall initiated | 2023-06-28 |
| Classified | 2023-08-17 |
| Reported by FDA | 2023-08-23 |
| Distributed | Nationwide (US) |
| Quantity | 44 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00763000624781 |
| Lot numbers | 226632942 |
| Model numbers | 46915 |
Product
Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only
Reason for recall
Product labeling contains incorrect expiration date
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-2412-2023. 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.