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Ferno-Washington Recalls
9 recalls on record · January 28, 2015 to July 29, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 29, 2026Medical DevicesFDA
Ferno-Washington Inc recalls Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use only. De
Hazard: Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. In the worst-case condition, rail mechanism may become lodged during operation and movement of the stretcher along the rail may no longer be possible through either powered or manual operation. May cause delays in transport of patient to healthcare facility.
October 22, 2025Medical DevicesFDA
Ferno-Washington Inc recalls FERNO POWER X2 POWERED AMBULANCE COT, Model/Catalog Number: 0015816; FOR USE IN GROUND TRANSPORTATION AMBULANCES.
Hazard: The fastening post hardware could loosen allowing the fastening post to detach from the cot
November 16, 2022Medical DevicesFDA
Ferno-Washington Inc recalls FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V Li-Ion Batteries Model Number #0822484/0822
Hazard: 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
April 26, 2017Medical DevicesFDA
Ferno-Washington Inc recalls Ferno PROFlexx¿ Model 28Z Chair Cot
Hazard: The recall was initiated as a result of the detection of an incorrect nut used in manufacturing.
May 11, 2016Medical DevicesFDA
Ferno-Washington Inc recalls Poly-bags containing the strap labeled with "Adult" sticker. Each strap kit contains adjustable length leg straps, an
Hazard: 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
May 11, 2016Medical DevicesFDA
Ferno-Washington Inc recalls Poly-bags containing splint strap labeled with "Pediatric" sticker. Each strap kit contains adjustable length leg str
Hazard: 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
October 7, 2015Medical DevicesFDA
Ferno-Washington Inc recalls Ferno iNX Wheeled Stretcher, Integrated Patient Transport & Loading System Product Usage: Stretcher for pre-hospital
Hazard: 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.
September 2, 2015Medical DevicesFDA
Ferno-Washington Inc recalls Wheel caster set screw for Ferno iNX Wheeled Stretcher. Ferno iNX Wheeled Stretcher for pre-hospital patient transport.
Hazard: 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.
January 28, 2015Medical DevicesFDA
Ferno-Washington Inc recalls Ferno Model 35X PROFlexx Stretchers, one unit per package
Hazard: The wheel castor assemblies may be loosening on the stretchers.