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.
mo-Vis BVBA is recalling the IDM-MICRO-R electrical wheelchair component because specific firmware versions may cause the device to skip a safety check. This error can lead to the wheelchair moving unexpectedly when powered on if the joystick is not in the neutral position. The recall affects 15 units distributed in Texas. Read more at govinfonow.com/recall/51816-mo-vis-electrical-wheelchair-component-recall-timing-issues-cause-unintended.
“mo-Vis IDM-MICRO-R Recall: Unintended Wheelchair Movement Hazard.” GovInfoNow, updated October 13, 2026. https://govinfonow.com/recall/51816-mo-vis-electrical-wheelchair-component-recall-timing-issues-cause-unintended. Based on FDA recall #Z-2456-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2456-2025%22&limit=1).
The FDA announced on July 10, 2025, that mo-Vis BVBA is recalling the IDM-MICRO-R electrical wheelchair component due to unintended movement risks. The agency issued recall number Z-2456-2025 for the Class I voluntary recall.
How to tell if you have it
Brand: mo-Vis
Product: IDM-MICRO-R
Model No.: PRSPS0014
UDI-DI: 05407008320836
Serial No.: 1000 to 1690
The hazard
Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check. This could cause the wheelchair to produce unintended movement upon power-up when the joystick is out of neutral.
Context
GovInfoNow's records show mo-Vis BVBA has one other recall on record since November 28, 2023, involving a throttle stuck risk in the Scoot Control R-net. Other recent recalls of similar products include Munevo Powered Wheelchair Hands-Free Control Software Issue May Cause Steering Drift (June 19, 2026), Quantum 4Front 2 Wheelchair: Reminder Pop-Ups May Cause Unexpected Stops (June 25, 2026), and Quantum Rehab 4Front Wheelchair Software 2.0.11 May Cause Unexpected Stops (June 25, 2026).
How to tell if you have this one
Check if your device is an IDM-MICRO-R electrical wheelchair component with Model No. PRSPS0014 and UDI-DI 05407008320836. Verify if the serial number falls between 1000 and 1690. These units were distributed nationwide in the state of TX.
Brand
mo-Vis
Category
Medical device
FDA recall event · 6 products
All 6 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class I
Status
Ongoing
Distribution
US Nationwide distribution in the state of TX.
Recall number
Product, codes & lots
Quantity
Z-2454-2025
Micro Joystick R-net. Electrical wheelchair component.; Model No. P002-52; UDI-DI: 05407008320027; Serial No. 1000 to 1690.
3 units
Z-2455-2025
Multi Joystick R-net. Electrical wheelchair component.; Model No. P002-62; UDI-DI: 05407008320041; Serial No. 1000 to 1690.
3 units
Z-2456-2025
IDM-MICRO-R. Electrical wheelchair component.; Model No. PRSPS0014; UDI-DI: 05407008320836; Serial No. 1000 to 1690.
15 units
Z-2457-2025
IDM-MULTI-R. Electrical wheelchair component.; Model No. PRSPS0016; UDI-DI: 05407008320850; Serial No. 1000 to 1690.
15 units
Z-2458-2025
All-round Joystick R-net Light. Electrical wheelchair component.; Model No. P002-76; UDI-DI: 05407008320096; Serial No. 1000 to 2647.
3 units
Z-2459-2025
IDM-ARLITE-R. Electrical wheelchair component.; Model No. PRSPS00018. UDI-DI: 05407008320102; Serial No. 1000 to 2647.
25 units
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution in the state of TX.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2456-2025 (July 10, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2456-2025 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 13, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.