BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2132436 · Received June 14, 2011

    Report

    Report Number
    1824206-2011-03248
    Event Type
    Malfunction
    Date Received
    June 14, 2011
    Date of Event
    June 1, 2011
    Report Date
    June 1, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECH FOUND THAT THE BRAKE CASTER WOULD LOCK AND HOLD, BUT BRAKE CASTER WOULD ROTATE IF PUSHED ON SIDE. REPLACED CASTER TO RESOLVE THIS ISSUE. BED FOUND ON FIRST FLOOR.

    Description of Event or Problem · 1

    COMPLAINT ALLEGED THAT THE BRAKE CASTER WOULD ROTATE IF PUSHED ON SIDE. NO PT INJURED. BED ON FIRST FLOOR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. P8000

    Patients

    Seq Age Sex Outcome Treatment
    1