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 recall was initiated as a result of the detection of an incorrect nut used in manufacturing. |
| Product | Ferno PROFlexx® Model 28Z Chair Cot |
| Quantity | 34 units |
| Distribution | Worldwide distribution. The recalled products were distributed to the following states: CA, FL, HI, IL, NY, OH. There are no government accounts for this recall. There are no Canada accounts for this recall. There are no Mexico accounts for this recall. The recalled product was distributed to the following countries: Taiwan, United Arab Emirates, Thailand, Singapore |
| Initiated | 2017-03-08 |
| Classified | 2017-04-15 |
| Terminated | 2017-06-29 |
| Recall number | Z-1827-2017 |
| 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-1827-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/76765/
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