Vanta/Seqenita LT Clinician Programmer Application — Class II medical device recall Z-0915-2023
Ongoing recall by Medtronic Neuromodulation, reported 2023-01-18. Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System
| Recall number | Z-0915-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Neuromodulation, Minneapolis, MN, United States |
| Recall initiated | 2022-12-03 |
| Classified | 2023-01-06 |
| Reported by FDA | 2023-01-18 |
| Quantity | 22 units |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 00763000447090 |
| Lot numbers | NPL3021964, NPL3021984, NPL3021990, NPL3022034, NPL3022043, NPL3022044, NPL3022049, NPL3022050, NPL3022052, NPL3022187, NPL3022190, NPL3022191, NPL3022193, NPL3022194, NPL3022195, NPL3022212, NPL3022213, NPL3022289, NPL3022795, NPL3022817, NPL3022869, NPL3022873 |
| Model numbers | CT900E |
Product
Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900E
Reason for recall
Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303"
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-0915-2023. 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.