Medtronic InterStim Ground Pad REF 041826 — Class II medical device recall Z-2365-2023
Ongoing recall by Medtronic Neuromodulation, reported 2023-08-16. Lot of InterStim Self-Adhesive Ground Pad is being recalled due to the product being labeled with the incorrec
| Recall number | Z-2365-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Neuromodulation, Minneapolis, MN, United States |
| Recall initiated | 2023-07-06 |
| Classified | 2023-08-10 |
| Reported by FDA | 2023-08-16 |
| Countries outside the US | IR |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 20763000343273 |
| Lot numbers | 60347246 |
| Model numbers | 041826 |
Product
Medtronic InterStim Ground Pad REF 041826
Reason for recall
Lot of InterStim Self-Adhesive Ground Pad is being recalled due to the product being labeled with the 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-2365-2023. 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.