BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FERNO-WASHINGTON, INC

    MDR report key: 453384 · Received April 10, 2003

    Report

    Report Number
    453384
    Event Type
    Malfunction
    Date Received
    April 10, 2003
    Date of Event
    March 22, 2003
    Report Date
    April 10, 2003
    Manufacturer
    FERNO-WASHINGTON, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    NY, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    STRETCHER WAS IN THE UPPER-MOST TRANSPORT POSITION, WHEN THE HANDLES WERE PULLED TO RELEASE THE WHEELS. THE WHEELS DID NOT RELEASE. STRETCHER WAS BOUNCED AROUND AND THE WHEELS FINALLY RELEASED, BUT THE STRETCHER WENT ALL THE WAY TO THE FLOOR AND WOULD NOT COME BACK UP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FERNO-WASHINGTON, INC STRETCHER FPO FERNO-WASHINGTON, INC. 79M *

    Patients

    Seq Age Sex Outcome Treatment
    1 87 YR