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Sign in to claim this brandFerno-Washington, Inc.
US
Last updated September 17, 2026
What Ferno-Washington, Inc. makes
Ferno-Washington, Inc. manufactures manual and electrohydraulic ambulance stretchers, including models designed for patient transport in emergency and medical settings. Their product line also includes stair chairs and cot-style devices, some of which are equipped for specialized transport, such as neonatal incubators. Additional offerings include modular transporter systems for moving patients between care environments.
The company’s devices are classified under FDA categories Class I and Class II, with regulatory authorisation through 510(k) clearances and inclusion in the FDA’s Unique Device Identifier (UDI) database. These products are listed under U.S. regulatory frameworks and are intended for use within the American healthcare system.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
- 70 WEIL WAY, Wilmington, OH, 45177
- Website
- ww.ferno.com
This website had an invalid or expired security certificate when we last checked. Last checked 2026-09-18.
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- Phone
- —
- PRRC Contact
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- EUDAMED SRN
- —
- FDA FEI Number
- 1523574
- DUNS Number
- —
Catalogue (150)
Page 2 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Mondial® Monobloc | 0054262 | FDA UDI | Class II | Active |
| York 4 Trolley | 0052200 | FDA UDI | Class II | Active |
| Mondial® Monobloc | 0054269 | FDA UDI | Class II | Unknown |
| Transcend Chair Series | 0731403 | FDA UDI | Class II | Active |
| iN∫X ® | 0015811 | FDA UDI | Class II | Active |
| PowerFlexx® | 0054215 | FDA UDI | Class II | Unknown |
| 25 Ambulance Cot | 0054082 | FDA UDI | Class II | Active |
| PowerFlexx® | 0015651 | FDA UDI | Class II | Unknown |
| 35X-ST ProFlexx® | 0015793 | FDA UDI | Class II | Unknown |
| 28Z ProFlexx® Chair Cot | 0012810 | FDA UDI | Class II | Active |
| 25 Ambulance Cot | 0054210 | FDA UDI | Class II | Unknown |
| Mondial® Monobloc | 0054252 | FDA UDI | Class II | Unknown |
| Mondial® Monobloc | 0054254 | FDA UDI | Class II | Unknown |
| Mondial® Transporter | 0054238 | FDA UDI | Class II | Active |
| PowerFlexx® | 0015729 | FDA UDI | Class II | Unknown |
| Mondial® Transporter | 0054222 | FDA UDI | Class II | Active |
| 93ES Squadmate® Ambulance Cot | 0015574 | FDA UDI | Class II | Unknown |
| 28A-1 Incubator Transporter | 0163283 | FDA UDI | Class II | Active |
| Mondial® Monobloc | 0054261 | FDA UDI | Class II | Active |
| 28A-1 Roll In Cot | 0163282 | FDA UDI | Class II | Unknown |
| 35X-ST ProFlexx® | 0015791 | FDA UDI | Class II | Unknown |
| 28Z MDA ProFlexx® Chair Cot | 0012825 | FDA UDI | Class II | Active |
| iN∫X ® | 0015808 | FDA UDI | Class II | Unknown |
| Mondial® Monobloc | 0054256 | FDA UDI | Class II | Active |
| 35A-IT Incubator Transporter | 0063120 | FDA UDI | Class II | Unknown |
| Mondial® Monobloc | 0054249 | FDA UDI | Class II | Unknown |
| 26P ProFlexx® | 0054208 | FDA UDI | Class II | Unknown |
| 35A-IT Incubator Transporter | 0063112 | FDA UDI | Class II | Unknown |
| PowerFlexx® Incubator Transporter | 0163272 | FDA UDI | Class II | Unknown |
| Mondial® Transporter | 0054229 | FDA UDI | Class II | Unknown |
| Mondial® Monobloc | 0054251 | FDA UDI | Class II | Unknown |
| Mondial® Monobloc | 0054263 | FDA UDI | Class II | Unknown |
| Mondial® Transporter | 0054274 | FDA UDI | Class II | Active |
| 50E Easy Load Stretcher | 0054134 | FDA UDI | Class II | Unknown |
| 146 Transport Incubator Folding Stand | 0063105 | FDA UDI | Class II | Unknown |
| 35X-IT ProFlexx® Incubator Transporter | 0163274 | FDA UDI | Class II | Unknown |
| Mondial® Transporter | 0054220 | FDA UDI | Class II | Unknown |
| iNX | 0015813 | FDA UDI | Class II | Unknown |
| Mondial® Monobloc | 0054253 | FDA UDI | Class II | Active |
| PowerFlexx® | 0015796 | FDA UDI | Class II | Unknown |
| 28A Roll In Cot | 0063099 | FDA UDI | Class II | Active |
| 4051 NT Transporter | 0054122 | FDA UDI | Class II | Unknown |
| Mondial® Monobloc | 0054247 | FDA UDI | Class II | Active |
| 35A-IT Incubator Transporter | 0063122 | FDA UDI | Class II | Unknown |
| 35A-XDF Ambulance Cot | 0015784 | FDA UDI | Class II | Unknown |
| Mondial® Transporter | 0054232 | FDA UDI | Class II | Active |
| 28Z ProFlexx® Chair Cot | 0012808 | FDA UDI | Class II | Unknown |
| Mondial® Transporter | 0054230 | FDA UDI | Class II | Unknown |
| Mondial® Monobloc | 0054250 | FDA UDI | Class II | Active |
| 35X-ST ProFlexx® | 0015790 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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FDA Recalls (12)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
Ferno-Washington, Inc. has 12 recall records initiated between March 28, 2003, and September 11, 2025, with statuses including open, classified, and terminated. The reasons cited involve manufacturing defects such as incorrect labeling on packaging for traction splint straps, improperly installed or incorrect hardware components (e.g., set screws, nuts, castings), potential structural failures (e.g., wheel castor loosening, stretcher folding, metal fatigue in legs), and design issues (e.g., hole elongation in telescoping load frames, improperly seated shank pins). Some records reference supplier errors in labeling, while others involve defects discovered during production or reported by users.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Sep 11, 2025 | Z-0133-2026 | — | open, classified | The fastening post hardware could loosen allowing the fastening post to detach from the cot |
| Oct 7, 2022 | Z-0184-2023 | — | open, classified | Batteries 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 |
| Mar 8, 2017 | Z-1827-2017 | — | terminated | The recall was initiated as a result of the detection of an incorrect nut used in manufacturing. |
| Mar 10, 2016 | Z-1603-2016 | — | terminated | On March 9, 2016, the firm was contacted regarding the possibility of incorrect labeling on the outside poly- bag of the traction splint straps. The firm investigated and determined its supplier had labeled the outside packaging for the pediatric and adult traction splints straps incorrectly. The packaging labeled Adult contained a pediatric splint strap and the packaging labeled pediatric cont |
| Mar 10, 2016 | Z-1604-2016 | — | terminated | On March 9, 2016, the firm was contacted regarding the possibility of incorrect labeling on the outside poly- bag of the traction splint straps. The firm investigated and determined its supplier had labeled the outside packaging for the pediatric and adult traction splints straps incorrectly. The packaging labeled Adult contained a pediatric splint strap and the packaging labeled Pediatric conta |
| Aug 3, 2015 | Z-2826-2015 | — | terminated | 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. |
| May 1, 2015 | Z-2461-2015 | — | terminated | 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. |
| Dec 3, 2014 | Z-0995-2015 | — | terminated | The wheel castor assemblies may be loosening on the stretchers. |
| Sep 3, 2008 | Z-2465-2008 | — | terminated | The Ferno Model 35-X PROFlexx legs could experience metal fatigue and possibly fracture after one to two years of use based on the usage and method of operation. |
| Apr 29, 2008 | Z-1859-2008 | — | terminated | A component defect was found in corner castings of the firm's wheeled ambulance stretchers. Some corner castings on the stretchers were found to be over-sized. Using an over-sized cone-shaped hole corner casting with an improperly seated shank pin could put undue stress on the top screw, possibly causing the screw securing a wheel to become loose or break and the wheel to detach from the stretcher |
| Mar 28, 2003 | Z-0202-06 | — | terminated | The firm received complaints of the stretchers folding. A fold is when the stretcher lowers on its own to either the next position, or any of the other seven postions of the stretcher. |
| Mar 28, 2003 | Z-0201-06 | — | terminated | The firm received complaints of the stretchers folding. A fold is when the stretcher lowers on its own to either the next position, or any of the other seven postions of the stretcher. |