Scoot Control R-net — Class II medical device recall Z-0713-2024
Ongoing recall by mo-Vis BVBA, reported 2024-01-17, distributed in TN, TX. In rare cases, the lever of the throttle can get temporarily stuck during the movement and does not come back
| Recall number | Z-0713-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | mo-Vis BVBA, Nevele, Belgium |
| Recall initiated | 2023-11-28 |
| Classified | 2024-01-11 |
| Reported by FDA | 2024-01-17 |
| Distributed | TN, TX |
| Quantity | 129 units |
| UPC / GTIN / UDI-DI | 05407008320119 |
| Lot numbers | 3304-3317, 3322-3329, 3440-3452, 3569-3618, 3830-3844, 4020-4054, 4170-4176, 4250-4255, 4321-4330 |
Product
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
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0713-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.