Class I — WHILL, INC.
| Recalling firm | WHILL, Inc. |
|---|---|
| Registered facility | WHILL, INC. (the firm's only registered facility) |
| Classification | Class I |
| Status | Ongoing |
| Reason | Cyber vulnerability of BLE communication was found by CISA VDP program. |
| 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. |
| Quantity | 2324 units |
| Distribution | US: Kansas |
| Initiated | 2025-12-29 |
| Classified | 2026-04-24 |
| Recall number | Z-1827-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class I recall — WHILL, INC. (Z-1827-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98320/
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