R-net Light Joystick (mo-Vis) – Software Timing Error (2025)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
All-round Joystick R-net Light. Electrical wheelchair component.
Brand
mo-Vis BVBA Biebuyckstraat 15D Nevele Belgium
Lot Codes / Batch Numbers
Model No. P002-76, UDI-DI: 05407008320096, Serial No. 1000 to 2647.
Products Sold
Model No. P002-76; UDI-DI: 05407008320096; Serial No. 1000 to 2647.
mo-Vis BVBA Biebuyckstraat 15D Nevele Belgium is recalling All-round Joystick R-net Light. Electrical wheelchair component. due to Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neu. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026