WHILL Model F — Class I medical device recall Z-1827-2026
Ongoing recall by WHILL, INC., reported 2026-05-06, distributed in KS. Cyber vulnerability of BLE communication was found by CISA VDP program.
| Recall number | Z-1827-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | WHILL, INC., Shinagawa, Japan |
| Recall initiated | 2025-12-29 |
| Classified | 2026-04-24 |
| Reported by FDA | 2026-05-06 |
| Distributed | KS |
| Quantity | 2,324 units |
| UPC / GTIN / UDI-DI | 04570072300019 |
| Serial numbers | FA1203U2220114, FA1203U2220115, FA1203U2220116, FA1203U2220117, FA1203U2220118, FA1203U2220119, FA1203U2220120, FA1203U2220121, FA1203U2220122, FA1203U2220123, FA1203U2220124, FA1203U2220125, FA1203U2220126, FA1203U2220127, FA1203U2220128, FA1203U2220129, FA1203U2220130, FA1203U2220131, FA1203U2220132, FA1203U2220133, FA1203U2220134, FA1203U2220135, FA1203U2220136, FA1203U2220137, FA1203U2220138 and 475 more |
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 for recall
Cyber vulnerability of BLE communication was found by CISA VDP program.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1827-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.