FDA Device recall Z-2226-2023
A901 Communication Manager Application, used in conjunction with the A710 Clinician Programmer application
- FDA Device
- Class II
- ongoing
- Published 2023-08-02
On 2023-08-02 the FDA classified a Class II recall of A901 Communication Manager Application, used in conjunction with the A710 Clinician Programmer application by Medtronic Neuromodulation, citing when an update to the A710 Clinician Programmer software application for the Intellis Neurostimulation System was released, the corresponding version of the A901 Communication Man….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2226-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-06-21 |
| Published | 2023-08-02 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medtronic Neuromodulation |
| Distribution | n/a |
Product
A901 Communication Manager Application, used in conjunction with the A710 Clinician Programmer application..
Reason
When an update to the A710 Clinician Programmer software application for the Intellis Neurostimulation System was released, the corresponding version of the A901 Communication Manager software application was not available for download.
Identifiers
| code_info | Serial numbers NPL3011706 and NPL3016791, UDI-DI 643169738058. |
|---|
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-2226-2023%22
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