FDA Medical devices recall ·
Multi Joystick R-net recall
This is an FDA Class I recall — the most serious type.
- Recall number
- Z-2455-2025
- Date
- (initiated July 10, 2025)
- Company / brand
- mo-Vis BVBA
Biebuyckstraat 15D, Nevele, N/A, Belgium - Category
- Medical devices › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 3 units
- Hazard tags
- Software
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Multi Joystick R-net. Electrical wheelchair component.
Why was it 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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Model No. P002-62; UDI-DI: 05407008320041; Serial No. 1000 to 1690.
Distribution
US Nationwide distribution in the state of TX.
States: Texas
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (medical devices), recall Z-2455-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.