FDA Medical Device Recalls (openFDA)
mo-Vis BVBA: IDM-ARLITE-R. Electrical wheelchair component.
- Recall number
- Z-2459-2025
- Recalling firm
- mo-Vis BVBA
- Product
- IDM-ARLITE-R. Electrical wheelchair component.
- Status
- Open, Classified
- Initiated
- 2025-07-10
- Posted
- 2025-09-02
- Terminated
- not on file
- 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.
- Root cause
- Device Design
- Action
- An URGENT: MEDICAL DEVICE RECALL R-NET JOYSTICKS notification dated 07/10/2025 was sent to consignees instructing them to upgrade affected devices according to the provided Annex 2 or by emailing contact@mo-vis.com to coordinate return. The software upgrade of affected devices should be conducted during the next scheduled annual maintenance of the joystick. These actions should be verified. Questions can be directed via email to contact@mo-vis.com or by phone at +32 9 335 28 60.
- Quantity
- 25 units
- Distribution
- US Nationwide distribution in the state of TX.
- Lot, serial or model codes
- Model No. PRSPS00018. UDI-DI: 05407008320102; Serial No. 1000 to 2647.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- KNN
- Firm FEI
- 3011795161
- Firm city
- Nevele
- Firm state
- not on file
- Firm country
- Belgium
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28