Class I

Medical Device Recall: 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.

WHILL, INC. · December 29, 2025

Reason for Recall

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

Distribution

US: Kansas

Quantity Affected

2324 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1827-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.