SenSight Connector Plug — Class II medical device recall Z-0121-2024
Ongoing recall by Medtronic Neuromodulation, reported 2023-10-25, distributed nationwide. Medtronic is requesting return of a small number of units of the SenSight Connector Plug, Model B31061, due to
| Recall number | Z-0121-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Neuromodulation, Minneapolis, MN, United States |
| Recall initiated | 2023-01-20 |
| Classified | 2023-10-18 |
| Reported by FDA | 2023-10-25 |
| Distributed | Nationwide (US) |
| Quantity | 65 devices |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00763000426576 |
| Lot numbers | 082U30721 |
| Model numbers | B31061 |
Product
SenSight Connector Plug, Model Number B31061.
Reason for recall
Medtronic is requesting return of a small number of units of the SenSight Connector Plug, Model B31061, due to a discrepancy in the Use By Date (UBD) printed on the label.
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-0121-2024. 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.