BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2863062 · Received November 1, 2012

    Report

    Report Number
    1824206-2012-07033
    Event Type
    Malfunction
    Date Received
    November 1, 2012
    Date of Event
    May 20, 2008
    Report Date
    May 20, 2008
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN ISOLATED THE ISSUE TO WORN CASTERS. HE REPLACED THE FOUR CASTERS TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE FOUR BRAKE CASTERS ARE NOT HOLDING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED, STRETCHER FPO HILL-ROM, INC. 8000

    Patients

    Seq Age Sex Outcome Treatment
    1