Clinician Programmer Application — Class II medical device recall Z-0201-2022
Ongoing recall by Medtronic Neuromodulation, reported 2021-11-10, distributed nationwide. A software anomaly may occur with the clinician programmer application.
| Recall number | Z-0201-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Neuromodulation, Minneapolis, MN, United States |
| Recall initiated | 2021-09-23 |
| Classified | 2021-11-04 |
| Reported by FDA | 2021-11-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CN, IN, JP, KR, NZ |
| Quantity | 3,302 |
| Reason classes | software |
| Model numbers | A610 |
Product
Clinician Programmer Application (CPA) model A610 Clinician Software Application
Reason for recall
A software anomaly may occur with the clinician programmer application.
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-0201-2022. 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.