FDA Device recall Z-1826-2026
WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13
- FDA Device
- Class I
- ongoing
- Published 2026-05-06
On 2026-05-06 the FDA classified a Class I recall of WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13 by Whill, citing cyber vulnerability of BLE communication was found by CISA VDP program.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1826-2026 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-12-29 |
| Published | 2026-05-06 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Whill |
| Distribution | KS |
Product
WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an indoor/outdoor battery-operated 2-wheel drive (rear-wheel drive) powered wheelchair.
Reason
Cyber vulnerability of BLE communication was found by CISA VDP program.
Identifiers
| code_info | UDI/DI 04570072300019, Serial Numbers: CB2307U25A0134, CB2307U25A0133, CB2307U25A0132, CB2307U25A0131, CB2307U25A0130,…UDI/DI 04570072300019, Serial Numbers: CB2307U25A0134, CB2307U25A0133, CB2307U25A0132, CB2307U25A0131, CB2307U25A0130, CB2307U25A0129, CB2307U25A0128, CB2307U25A0127, CB2307U25A0126, CB2307U25A0125, CB2307U25A0124, CB2307U25A0123, CB2307U25A0122, CB2307U25A0121, CB2307U25A0120, CB2307U25A0119, CB2307U25A0118, CB2307U25A0117, CB2307U25A0116, CB2307U25A0115, CB2207U25A0114, CB2207U25A0113, CB2207U25A0112, CB2207U25A0111, CB2207U25A0110, CB2207U25A0109, CB2207U25A0108, CB2207U25A0107, CB2207U25A0106, CB2207U25A0105, CB2207U25A0104, CB2207U25A0103, CB2207U25A0102, CB2207U25A0101, CB2207U25A0100, CB2207U25A0099, CB2207U25A0098, CB2207U25A0097, CB2207U25A0096, CB2207U25A0095, CB2207U25A0094, CB2207U25A0093, CB2207U25A0092, CB2207U25A0091, CB2207U25A0090, CB2207U25A0089, CB2207U25A0088, CB2207U25A0087, CB2107U25A0086, CB2107U25A0085, CB2107U25A0084, CB2107U25A0083, CB2107U25A0082, CB2107U25A0081, CB2107U25A0080, CB2107U25A0079, CB2107U25A0078, CB2107U25A0077, CB2107U25A0076, CB2107U25A0075, |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1826-2026%22
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