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CLASS I · SeriousFDA

WHILL, INC. recalls WHILL

📅 Dec 29, 2025 · 📍 KS
Recalling company
WHILL, INC.
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.
Reason
Cyber vulnerability of BLE communication was found by CISA VDP program.
Classification
Class I – a reasonable probability that use will cause serious adverse health consequences or death
Recall date
Dec 29, 2025
Reported
May 6, 2026
Distribution
US: Kansas
Status
Ongoing
Quantity
2324 units
Lot / codes
UDI/DI 04570072300019, Serial Numbers: FB1203U2610192, FB1203U2610191, FB1203U2610190, FB1203U2610189, FB1203U2610188, FB1203U2610187, FB1203U2610186, FB1203U2610185, FB1203U2610184, FB1203U2610183, FB1203U2610182, FB1203U2610181, FB1203U2610180, FB1203U2610179, FB1203U2610178, FB1203U2610177, FB1203U2610176, FB1203U2610175, FB1203U2610174, FB1203U2610173, FB1203U2610172, FB1203U2610171, FB1203U2610170, FB1203U2610169, FB1203U2610168, FB1203U2610167, FB1203U2610166, FB1203U2610165, FB1203U2610164, FB1203U2610163, FB1203U2610162, FB1203U2610161, FB1203U2610160, FB1203U2610159, FB1203U2610158, FB1203U2610157, FB1203U2610156, FB1203U2610155, FB1203U2610154, FB1203U2610153, FB1203U2610152, FB1203U2610151, FB1203U2610150, FB1203U2610149, FB1203U2610148, FB1203U2610147, FB1203U2610146, FB1203U2610145, FB1203U2610144, FB1203U2610143, FB1203U2610142, FB1203U2610141, FB1203U2610140, FB1203U2610139, FB1203U2610138, FB1203U2610137, FB1203U2610136, FB1203U2610135, FB1203U2610134, FB1203U2610133, FB1203U2610132, FB1203U2610131, FB1203U2610130, FB1203U2610129, FB1203U2610128, FB1203U2610127, FB1203U2610126, FB1203U2610125, FB1203U2610124, FB1203U2610123, FB1203U2610122, FB1203U2610121, FB1203U2610120, FB1203U2610119, FB1203U2610118, FB1203U2610117, FB1203U2610116, FB1203U2610115, FB1203U2610114, FB1203U2610113, FB1203U2610112, FB1203U2610111, FB1203U2610110, FB1203U2610109, FB1203U2610108, FB1203U2610107, FB1203U2610106, FB1203U2610105, FB1203U2610104, FB1203U2610103, FB1203U2610102, FB12
Company location
Shinagawa
Recall type
Voluntary: Firm initiated
Recall number
Z-1827-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-1827-2026 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.