Intellis AdaptiveStim Product Number 97715 — Class II medical device recall Z-1691-2024
Ongoing recall by Medtronic Neuromodulation, reported 2024-05-08. inability to reprogram one device
| Recall number | Z-1691-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Neuromodulation, Minneapolis, MN, United States |
| Recall initiated | 2024-03-28 |
| Classified | 2024-04-26 |
| Reported by FDA | 2024-05-08 |
| Countries outside the US | GB |
| Quantity | 1 units |
| UPC / GTIN / UDI-DI | 00643169781719 |
Product
Intellis AdaptiveStim Product Number 97715, Spinal Cord Stimulator
Reason for recall
inability to reprogram one device
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-1691-2024. 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.