# FDA recall Z-0184-2023

> **Ferno-Washington Inc** · Class II · device recall initiated 2022-10-07.

## Product

FERNO POWER X1 AMBULANCE COT-  Item #0015807/UDI-DI 00190790002183  with 36V Li-Ion Batteries Model Number #0822484/0822483    Note: Transcend Stair Chair Powertraxx (Item #0731403/UDI-DI 00190790004064)  not included in this action).

## Reason for recall

Batteries could become unstable when not properly maintained and/or subjected to repeated drops, power washing directly into battery contacts or abuse, may result in a fire and/or injury

## Distribution

Nationwide Foreign:  BRAZIL BRUNEI CHILE CHINA PERU POLAND PUERTO RICO TURKS&CACOS

## Key facts

- **Recall number:** Z-0184-2023
- **Recalling firm:** Ferno-Washington Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-10-07
- **Report date:** 2022-11-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Wilmington, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0184-2023

## Citation

> AI Analytics. FDA recall Z-0184-2023. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/Z-0184-2023. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*