Official recall notice
FDA DeviceClass INotable
FDA Recall: WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is an indoor/outdoor,
- Recall date
- 2026-05-06
- Brand
- WHILL, INC.
- Category
- Medical Device
- FDA class
- Class I
Why it was recalled
Hazard
Cyber vulnerability of BLE communication was found by CISA VDP program.
Recommended action
What to do
2324 units
Product description
Cyber vulnerability of BLE communication was found by CISA VDP program.