BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 3222045 · Received July 5, 2013

    Report

    Report Number
    1824206-2013-03361
    Event Type
    Malfunction
    Date Received
    July 5, 2013
    Date of Event
    June 10, 2013
    Report Date
    June 10, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT FOUND THE BRAKE LINKAGE WAS BROKEN. THE ACCOUNT REPLACED THE BRAKE LINKAGE TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE BRAKES ON THE HEAD END OF THE STRETCHER WOULD NOT HOLD. NO PATIENT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    307614 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8020

    Patients

    Seq Age Sex Outcome Treatment
    1