Vanta Implantable Neurostimulator — Class II medical device recall Z-0132-2025
Ongoing recall by Medtronic Neuromodulation, reported 2024-10-23. Model 977006 Vanta INS batterty life has depleted faster than HCPs or patients expected leading to outpatient
| Recall number | Z-0132-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Neuromodulation, Minneapolis, MN, United States |
| Recall initiated | 2024-08-21 |
| Classified | 2024-10-17 |
| Reported by FDA | 2024-10-23 |
| Quantity | 11,789 units |
| UPC / GTIN / UDI-DI | 00763000411923, 00763000478087, 00763000518615, 00763000754242, 00763000849078 |
| Serial numbers | 505523H, NMS5, NMS500093H, NMS500094H, NMS500095H, NMS500097H, NMS500098H, NMS500099H, NMS500100H, NMS500101H, NMS500102H, NMS500103H, NMS500104H, NMS500106H, NMS500107H, NMS500109H, NMS500110H, NMS500111H, NMS500113H, NMS500115H, NMS500116H, NMS500117H, NMS500118H, NMS500119H, NMS500121H and 475 more |
| Model numbers | 977006 |
Product
Vanta Implantable Neurostimulator (INS), Model 977006
Reason for recall
Model 977006 Vanta INS batterty life has depleted faster than HCPs or patients expected leading to outpatient reprogramming or earlier than anticipated surgical replacements.
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-0132-2025. 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.