FDA Device recall Z-0201-2022
Clinician Programmer Application (CPA) model A610 Clinician Software Application
- FDA Device
- Class II
- ongoing
- Published 2021-11-10
On 2021-11-10 the FDA classified a Class II recall of Clinician Programmer Application (CPA) model A610 Clinician Software Application by Medtronic Neuromodulation, citing A software anomaly may occur with the clinician programmer application.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0201-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-09-23 |
| Published | 2021-11-10 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medtronic Neuromodulation |
| Distribution | US |
Product
Clinician Programmer Application (CPA) model A610 Clinician Software Application
Reason
A software anomaly may occur with the clinician programmer application.
Identifiers
| code_info | Clinician Programmer Application (CPA) model A610 version 3.0.1048, 3.0.1057, 3.0.1062, and 3.0.1081 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0201-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.