BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2222421 · Received July 14, 2011

    Report

    Report Number
    1824206-2011-03727
    Event Type
    Malfunction
    Date Received
    July 14, 2011
    Date of Event
    July 7, 2011
    Report Date
    July 8, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECH FOUND THAT THE BRAKES WERE LOCKING, BUT WOULD SWIVEL FREE. REPLACED ALL CASTERS TO CORRECT THIS PROBLEM.

    Description of Event or Problem · 1

    COMPLAINT ALLEGED THAT THE STRETCHER BRAKES WERE NOT WORKING PROPERLY. ALL FOUR CASTER WHEELS WILL LOCK BUT SWIVEL FREE. NO INJURY ALLEGED.

    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