BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2132416 · Received June 14, 2011

    Report

    Report Number
    1824206-2011-03244
    Event Type
    Malfunction
    Date Received
    June 14, 2011
    Date of Event
    June 2, 2011
    Report Date
    June 2, 2011
    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

    TECHNICIAN FOUND THAT THE FOOT BRAKES WERE NOT HOLDING DUE TO BAD CASTERS. REPLACED FOOT BRAKE CASTERS TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    COMPLAINT ALLEGED THAT THE FOOT BRAKES WERE NOT HOLDING. 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