RegWardenFDA facility compliance records
Recall

Class II — Ferno-Washington Inc

Recalling firmFerno-Washington, Inc.
Registered facilityFERNO-WASHINGTON, INC. (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonBatteries 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
ProductFERNO 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).
Quantity1,922 units
DistributionNationwide Foreign: BRAZIL BRUNEI CHILE CHINA PERU POLAND PUERTO RICO TURKS&CACOS
Initiated2022-10-07
Classified2022-11-04
Recall numberZ-0184-2023
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Ferno-Washington Inc (Z-0184-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/90957/

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