Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2461-2015 — Wheel caster set screw for Ferno iNX Wheeled Stretcher. Ferno iNX Wheeled Stretcher for pre-hospital patient transport.

U.S. FDA — Device Enforcement · United States · 2015-05-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2461-2015
Date of alert
2015-05-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ferno-Washington Inc
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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