PlainRecalls
FDA Devices Critical Class I Ongoing

IDM-MICRO-R. Electrical wheelchair component.

Reported: September 10, 2025 Initiated: July 10, 2025 #Z-2456-2025

Product Description

IDM-MICRO-R. Electrical wheelchair component.

Reason for Recall

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.

Details

Recalling Firm
mo-Vis BVBA
Units Affected
15 units
Distribution
US Nationwide distribution in the state of TX.
Location
Nevele, N/A

Frequently Asked Questions

What product was recalled?
IDM-MICRO-R. Electrical wheelchair component.. Recalled by mo-Vis BVBA. Units affected: 15 units.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 10, 2025. Severity: Critical. Recall number: Z-2456-2025.