Medtronic Percept RC Implantable Neurostimulators — Class II medical device recall Z-0206-2025
Ongoing recall by Medtronic Neuromodulation, reported 2024-10-30. A limited number of Percept RC Implantable Neurostimulators (INS), Model B35300 will not be able to communicat
| Recall number | Z-0206-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Neuromodulation, Minneapolis, MN, United States |
| Recall initiated | 2024-09-24 |
| Classified | 2024-10-23 |
| Reported by FDA | 2024-10-30 |
| Countries outside the US | DE, GB, IL |
| Quantity | 39 units |
| UPC / GTIN / UDI-DI | 00763000813468, 00763000813475, 00763000813529, 07630008135201 |
| Serial numbers | NND504156H, NND504157H, NND504159H, NND504160H, NND504165H, NND504167H, NND504169H, NND504174H, NND504178H, NND504179H, NND504180H, NND504181H, NND504182H, NND504208H, NND504212H, NND504215H, NND504216H, NND504217H, NND504218H, NND504221H, NND504222H, NND504223H, NND504224H, NND504227H, NND504228H and 9 more |
| Model numbers | B35300 |
Product
Medtronic Percept RC Implantable Neurostimulators (INS), Model B35300.
Reason for recall
A limited number of Percept RC Implantable Neurostimulators (INS), Model B35300 will not be able to communicate with the A610 DBS Clinician Programmer Application upon use and an "Invalid Device" message will appear.
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-0206-2025. 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.