FDA Device recall Z-2456-2025
IDM-MICRO-R. Electrical wheelchair component
- FDA Device
- Class I
- ongoing
- Published 2025-09-10
On 2025-09-10 the FDA classified a Class I recall of IDM-MICRO-R. Electrical wheelchair component by Mo Vis Bvba, citing devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2456-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-07-10 |
| Published | 2025-09-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Mo Vis Bvba |
| Distribution | US |
Product
IDM-MICRO-R. Electrical wheelchair component.
Reason
Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
Identifiers
| code_info | Model No. PRSPS0014; UDI-DI: 05407008320836; Serial No. 1000 to 1690. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2456-2025%22
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