CLASS I ONGOING Device recall · Reported 10 Sep 2025 · FDA Enforcement Report
All-round Joystick R-net Light recalled by mo-Vis BVBA
mo-Vis BVBA is recalling All-round Joystick R-net Light, distributed nationwide in the US. The recall was initiated on 10 Jul 2025 and the FDA has classified it as Class I.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2458-2025
- FDA event ID
- 97354
- Recalling firm
- mo-Vis BVBA, Nevele, N/A
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 10 Jul 2025
- FDA classified
- 2 Sep 2025
- Reported
- 10 Sep 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Device Malfunction
- Device type
- Wheelchairs, Beds & Lifts
Timeline
| 10 Jul 2025 | Recall initiated by company | |
| 2 Sep 2025 | Classified by FDA | +54 days |
| 10 Sep 2025 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
All-round Joystick R-net Light. Electrical wheelchair component.
Where it was distributed
US Nationwide distribution in the state of TX.
Questions about this recall
Is All-round Joystick R-net Light recalled?
Yes. mo-Vis BVBA recalled All-round Joystick R-net Light on 10 Jul 2025. The recall is Class I and its status is Ongoing. Recall number Z-2458-2025.
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.
Which lots are affected?
Model No. P002-76; UDI-DI: 05407008320096; Serial No. 1000 to 2647.
Where was it sold?
US Nationwide distribution in the state of TX.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from mo-Vis BVBA
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | Multi Joystick R-net recalled by mo-Vis BVBA | mo-Vis BVBA | Device Malfunction | Nationwide |
| Device | CLASS I | Idm-multi-r. Electrical wheelchair component recalled by mo-Vis BVBA | mo-Vis BVBA | Device Malfunction | Nationwide |
| Device | CLASS I | Idm-arlite-r. Electrical wheelchair component recalled by mo-Vis BVBA | mo-Vis BVBA | Device Malfunction | Nationwide |
| Device | CLASS I | Micro Joystick R-net recalled by mo-Vis BVBA | mo-Vis BVBA | Device Malfunction | Nationwide |
| Device | CLASS I | Idm-micro-r. Electrical wheelchair component recalled by mo-Vis BVBA | mo-Vis BVBA | Device Malfunction | Nationwide |
Other Wheelchairs, Beds & Lifts recalls
All 172| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Quantum Rehab Quantum 4Front 2HD recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge 0 (ilevel) recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |