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 wheel castor assemblies may be loosening on the stretchers. |
| Product | Ferno Model 35X PROFlexx Stretchers, one unit per package |
| Quantity | 46 units |
| Distribution | The affected product was distributed to the following states: OH, MA, HI, NJ, TN, TX, MO, and GA. The affected product was distributed to the following foreign countries: Canada, Germany and Venezuela. |
| Initiated | 2014-12-03 |
| Classified | 2015-01-16 |
| Terminated | 2015-12-01 |
| Recall number | Z-0995-2015 |
| 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-0995-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/69978/
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