WHILL, INC. recalls WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is an indoor/outdoor, foldable battery-ope

Recalled May 6, 2026 · FDA recall Z-1827-2026 · WHILL

Hazard

Cyber vulnerability of BLE communication was found by CISA VDP program. · FDA Class I

Units

2324 units

Sold at

US: Kansas

Description

Cyber vulnerability of BLE communication was found by CISA VDP program.

Product

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.

Manufacturer(s)

WHILL, INC.

Made in

Japan

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →