# FDA recall Z-1827-2026

> **WHILL, INC.** · Class I · device recall initiated 2025-12-29.

## 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.

## Distribution

US: Kansas

## Key facts

- **Recall number:** Z-1827-2026
- **Recalling firm:** WHILL, INC.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-29
- **Report date:** 2026-05-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Shinagawa, Japan

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1827-2026

## Citation

> AI Analytics. FDA recall Z-1827-2026. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-1827-2026. Source: US FDA. Licensed CC0.

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