Shinagawa, Japan
WHILL, INC. recalls
1 recall recorded since 2018, most recently on 29 December 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)1
Ongoing Class I Medical devices
- Recall started
- 29 December 2025
- Reason
- Cyber vulnerability of BLE communication was found by CISA VDP program.
- Distribution
- US: Kansas
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1826-2026, Z-1827-2026
- WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an indoor/outdoor battery-operated 2-wheel drive (rear-wheel drive) powered wheelchair.
- WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is an indoor/outdoor, foldable battery-operated 2-wheel drive (rear-wheel drive) powered wheelchair.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.