BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2031752 · Received March 21, 2011

    Report

    Report Number
    1824206-2011-01722
    Event Type
    Malfunction
    Date Received
    March 21, 2011
    Date of Event
    March 2, 2011
    Report Date
    March 2, 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

    TECHNICIAN FOUND THE STRETCHER IN MAINTENANCE. NO INJURY WAS REPORTED. REPLACED THE CASTERS TO RESOLVE THE PROBLEM.

    Description of Event or Problem · 1

    COMPLAINANT ALLEGED THAT WHEN THE BRAKES WERE SET THAT THE CASTER WHEEL WILL NOT ROLL, BUT STILL ROTATES AROUND.

    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