Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1827-2026 — 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.

U.S. FDA — Device Enforcement · Japan · 2025-12-29 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1827-2026
Date of alert
2025-12-29
Country / jurisdiction
Japan
Risk level
Class I
Risk type
recall
Brand
WHILL, INC.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04570072300019
Reported risk: Cyber vulnerability of BLE communication was found by CISA VDP program.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.