Critical Alert
WHILL Recalls WHILL Model F
This is a Class I recall — the most serious type. There is a reasonable probability of serious health consequences or death.
Source: FDA
CriticalRecall #Z-1827-2026Medical Device
WHILL Recalls WHILL Model F
WHILL, INC. · Class I — Most Serious
Product 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.
Reason for Recall
Cyber vulnerability of BLE communication was found by CISA VDP program.
FDA Classification
Class I — Most Serious
A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Distribution
US: Kansas
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
WHILL, INC. is recalling a medical device classified as Class I by the FDA — the highest risk level. The recall was initiated on December 29, 2025 affecting 2324 units. Cyber vulnerability of BLE communication was found by CISA VDP program. It was distributed in US: Kansas. Consumers and healthcare professionals should exercise caution and discontinue use of the recalled product. Contact the recalling firm directly for return or disposal instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Other Injury Hazards.