Medical Device

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

Recall date: 2026-05-06 · Source: FDA_DEVICE

Brand / Firm

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.

Reason for recall

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

Units affected

2324 units

Description

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.

View official recall notice →