RecallRadar

FDA Device recall Z-2461-2015

Wheel caster set screw for Ferno iNX Wheeled Stretcher

On 2015-09-02 the FDA classified a Class II recall of Wheel caster set screw for Ferno iNX Wheeled Stretcher by Ferno Washington, citing 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 fr….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2461-2015
ClassificationClass II
Statusterminated
Initiated2015-05-01
Published2015-09-02
Last updated2026-09-13 11:53 UTC
CompanyFerno Washington
DistributionAZ, CO, IA, MD, OH, PA, WA

Product

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

Reason

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.

Identifiers

code_info
Serial numbers: 15F001703, 15F001704, 15F001705, 15F001706, 15F001707, 15F001708, 15F001709, 15F001710, 15F001711, 15F0…Serial numbers: 15F001703, 15F001704, 15F001705, 15F001706, 15F001707, 15F001708, 15F001709, 15F001710, 15F001711, 15F001712, 15F001713, 15F001714, 15F001715, 15F001716, 15F001717, 15F001719, 15F001720, 15F001721, 15F001722, 15F001723, 15F001724, 15F001725, 15F001726, 15F001727, 15F001729 & 15F001730.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2461-2015%22

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