# FDA recall Z-0713-2024

> **mo-Vis BVBA** · Class II · device recall initiated 2023-11-28.

## 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.

## Distribution

US States: TN, TX.

## Key facts

- **Recall number:** Z-0713-2024
- **Recalling firm:** mo-Vis BVBA
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-28
- **Report date:** 2024-01-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Nevele, Belgium

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0713-2024

## Citation

> AI Analytics. FDA recall Z-0713-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0713-2024. Source: US FDA. Licensed CC0.

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