CLASS II ONGOING Device recall · Reported 17 Jan 2024 · FDA Enforcement Report
Scoot Control R-net, Product Number P015 recalled by mo-Vis BVBA
mo-Vis Bvba is recalling Scoot Control R-net, Product Number P015-61, distributed in Tennessee, Texas. The recall was initiated on 28 Nov 2023 and the FDA has classified it as Class II.
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-0713-2024
- FDA event ID
- 93556
- Recalling firm
- mo-Vis Bvba, Nevele
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 28 Nov 2023
- FDA classified
- 11 Jan 2024
- Reported
- 17 Jan 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Device Malfunction
- Device type
- Wheelchairs, Beds & Lifts
Timeline
| 28 Nov 2023 | Recall initiated by company | |
| 11 Jan 2024 | Classified by FDA | +44 days |
| 17 Jan 2024 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
In rare cases, the lever of the throttle can get temporarily stuck during the movement and does not come back to its neutral point by itself. If this happens during usage, an unwanted movement of the chair could be the result. An unwanted movement could result in damage to the wheelchair, material damage around the chair and/or injury to the user, attendant or by-standers.
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
Scoot Control R-net, Product Number P015-61. The Scoot Control is intended to support a wheelchair attendant in controlling or maneuvering a power chair
Where it was distributed
US States: TN, TX.
Questions about this recall
Why was it recalled?
In rare cases, the lever of the throttle can get temporarily stuck during the movement and does not come back to its neutral point by itself. If this happens during usage, an unwanted movement of the chair could be the result. An unwanted movement could result in damage to the wheelchair, material damage around the chair and/or injury to the user, attendant or by-standers.
Which lots are affected?
UDI-DI: 05407008320119; Lot Numbers: 3304-3317 3322-3329 3440-3452 3569-3618 3830-3844 4020-4054 4170-4176 4250-4255 4321-4330
Where was it sold?
US States: TN, 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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 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 | All-round Joystick R-net Light 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 |
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 2.0 (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 |