Medical device recalls Moderate risk

Ferno-Washington Inc recalls Wheel caster set screw for Ferno iNX Wheeled Stretcher. Ferno iNX Wheeled Stretcher for pre-hospital patient transport.

Recall date
May 1, 2015
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2461-2015
FDA classification
Class II
Brand / firm
Ferno-Washington Inc
Sold / distributed
Distributed in the states of AZ, CO, IA, MD, OH, PA & WA, and the countries of Australia, Canada & United Kingdom.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Wheel caster set screw for Ferno iNX Wheeled Stretcher. Ferno iNX Wheeled Stretcher for pre-hospital patient transport.

Get recall alerts

Free email alert whenever Ferno-Washington Inc has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Ferno-Washington Inc