Class II — Ferno-Washington Inc
| Recalling firm | Ferno-Washington, Inc. |
|---|---|
| Registered facility | FERNO-WASHINGTON, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The firm discovered an improperly installed set screw in one caster arm assembly on a unit in production. The screw assists in preventing the bearing cup on the caster assembly from backing out of the caster arm during use. |
| Product | Wheel caster set screw for Ferno iNX Wheeled Stretcher. Ferno iNX Wheeled Stretcher for pre-hospital patient transport. |
| Quantity | 26 units |
| Distribution | Distributed in the states of AZ, CO, IA, MD, OH, PA & WA, and the countries of Australia, Canada & United Kingdom. |
| Initiated | 2015-05-01 |
| Classified | 2015-08-25 |
| Terminated | 2015-11-06 |
| Recall number | Z-2461-2015 |
| Initiation | Voluntary: 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-2461-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/71556/
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