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Ferno-Washington, Inc.

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.
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 1523574
DUNS Number: —

Catalogue (150)

Page 1 of 3

Device	Model / Reference	Registries	Class	Status
35X ProFlexx®	0015690	FDA UDI	Class II	Active
5226EL Cot	0054213	FDA UDI	Class II	Unknown
Mondial® Monobloc	0054246	FDA UDI	Class II	Active
Mondial® Monobloc	0054260	FDA UDI	Class II	Unknown
4051 Transporter	0054099	FDA UDI	Class II	Unknown
Mondial® Monobloc	0054258	FDA UDI	Class II	Active
Mondial® Transporter	0054240	FDA UDI	Class II	Unknown
Mondial® Monobloc	0054264	FDA UDI	Class II	Unknown
PowerFlexx 1.25	0015804	FDA UDI	Class II	Unknown
35X-IT ProFlexx® Incubator Transporter	0163273	FDA UDI	Class II	Active
35A Ambulance Cot	0012079	FDA UDI	Class II	Unknown
35X-IT ProFlexx® Incubator Transporter	0163275	FDA UDI	Class II	Unknown
4052 NT Transporter	0054121	FDA UDI	Class II	Unknown
iNX	0015802	FDA UDI	Class II	Unknown
Mondial® Monobloc	0054255	FDA UDI	Class II	Unknown
4052 G Transporter	0054125	FDA UDI	Class II	Unknown
Mondial® Monobloc	0054259	FDA UDI	Class II	Unknown
Mondial® Transporter	0054235	FDA UDI	Class II	Unknown
PowerFlexx®	0015730	FDA UDI	Class II	Unknown
26S Cot	0053976	FDA UDI	Class II	Active
Mondial® Monobloc	0054266	FDA UDI	Class II	Unknown
PowerFlexx®	0015799	FDA UDI	Class II	Unknown
PowerFlexx® Incubator Transporter	0163271	FDA UDI	Class II	Unknown
93H ProFlexx®	0015762	FDA UDI	Class II	Unknown
Mondial® Transporter	0054276	FDA UDI	Class II	Active
iN∫X ®	0015810	FDA UDI	Class II	Unknown
Power X2	0015816	FDA UDI	Class II	Active
Mondial® Transporter	0054243	FDA UDI	Class II	Unknown
PowerFlexx® Incubator Transporter	0163280	FDA UDI	Class II	Unknown
35X ProFlexx®	0015703	FDA UDI	Class II	Unknown
35X-NM ProFlexx®	0015788	FDA UDI	Class II	Active
26 Cot	0012600	FDA UDI	Class II	Unknown
28Z ProFlexx® Chair Cot	0012805	FDA UDI	Class II	Active
Mondial® Transporter	0054241	FDA UDI	Class II	Active
Mondial® Transporter	0054228	FDA UDI	Class II	Active
PowerFlexx®	0054216	FDA UDI	Class II	Unknown
Mondial® Monobloc	0054265	FDA UDI	Class II	Unknown
26T Ambulance Cot	0051205	FDA UDI	Class II	Unknown
Transcend Chair Series	0731401	FDA UDI	Class I	Active
35X ProFlexx®	0015693	FDA UDI	Class II	Unknown
Transcend Evacuation Chair	0731404	FDA UDI	Class I	Active
PowerFlexx® Incubator Transporter	0163278	FDA UDI	Class II	Unknown
Transcend	0731405	FDA UDI	Class II	Active
93-IT Incubator Transporter	0063114	FDA UDI	Class II	Unknown
28A-1 Incubator Transporter	0163284	FDA UDI	Class II	Unknown
Mondial® Transporter	0054242	FDA UDI	Class II	Unknown
PowerFlexx®	0015797	FDA UDI	Class II	Unknown
iNX	0015809	FDA UDI	Class II	Unknown
93-IT Incubator Transporter	0063115	FDA UDI	Class II	Unknown
PowerFlexx®	0015726	FDA UDI	Class II	Unknown

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.