# FDA recall Z-2458-2025

> **mo-Vis BVBA** · Class I · device recall initiated 2025-07-10.

## Product

All-round Joystick R-net Light. Electrical wheelchair component.

## 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.

## Distribution

US Nationwide distribution in the state of TX.

## Key facts

- **Recall number:** Z-2458-2025
- **Recalling firm:** mo-Vis BVBA
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-10
- **Report date:** 2025-09-10

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2458-2025

## Citation

> AI Analytics. FDA recall Z-2458-2025. Retrieved 2026-08-12 from https://api.ai-analytics.org/recall/Z-2458-2025. Source: US FDA. Licensed CC0.

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