Data Foundry

Medical device recalls 2026

WHILL Model C2 — Class I medical device recall Z-1826-2026

Ongoing recall by WHILL, INC., reported 2026-05-06, distributed in KS. Cyber vulnerability of BLE communication was found by CISA VDP program.

Recall numberZ-1826-2026
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmWHILL, INC., Shinagawa, Japan
Recall initiated2025-12-29
Classified2026-04-24
Reported by FDA2026-05-06
DistributedKS
Quantity4,685 units
UPC / GTIN / UDI-DI04570072300019
Serial numbersCB2107U22B0269, CB2107U22B0270, CB2107U22B0271, CB2107U22B0272, CB2107U22B0273, CB2107U22B0274, CB2107U22B0275, CB2107U22B0276, CB2107U22B0277, CB2107U22B0278, CB2107U22B0279, CB2107U22B0280, CB2107U22B0281, CB2107U22B0282, CB2107U22B0283, CB2107U22B0284, CB2107U22B0285, CB2107U22B0286, CB2107U22B0287, CB2107U22B0288, CB2107U22B0289, CB2107U22B0290, CB2107U22B0291, CB2107U22B0292, CB2107U22B0293 and 475 more

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 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-1826-2026. 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.