Recall Z-0184-2023— Ferno-Washington Inc
Class II · Ongoing
Class II FDA medical device recall by Ferno-Washington Inc, initiated 2022-10-07. FDA's recall record names no specific 510(k) clearance for this event. 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: 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.
- Recalling firm
- Ferno-Washington Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-10-07
- Firm location
- Wilmington, OH, United States
Product description
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
Data sourced from openFDA. This site is unofficial and independent of the FDA.