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 | Hole elongation in the telescoping load frame channel. A hole elongation could affect the ability of the retention pin to stay seated which is necessary to preclude movement of the telescoping load frame. |
| Product | Ferno iNX Wheeled Stretcher, Integrated Patient Transport & Loading System Product Usage: Stretcher for pre-hospital patient transport. |
| Quantity | 72 units |
| Distribution | Worldwide Distribution - US Nationwide in the states of: CO, IA, IL, IN, KY, MD, MN, MO, NC, NJ, NY, OH, OK, OR, TX, VA, WA & WY and the countries of CANADA, AUSTRALIA, UNITED KINGDOM & NEW ZEALAND. |
| Initiated | 2015-08-03 |
| Classified | 2015-09-30 |
| Terminated | 2016-01-20 |
| Recall number | Z-2826-2015 |
| 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-2826-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/71983/
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