FDADecember 29, 2025device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

whill

UPCs

04570072300019

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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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. — Recall Details · AllClear