BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 3071020 · Received April 8, 2013

    Report

    Report Number
    1824206-2013-01994
    Event Type
    Malfunction
    Date Received
    April 8, 2013
    Date of Event
    March 10, 2013
    Report Date
    March 10, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT FOUND THE CAUSE TO BE A BROKEN BRAKE PEDAL LINKAGE. THE ACCOUNT INSTALLED A BRAKE STEER UPGRADE KIT TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THAT THE FOOT BRAKE PEDAL DOES GO INTO BRAKE MODE AND IT APPEARS THE BRAKES ARE SET HOWEVER THE FOOT END BRAKE CASTERS DO NOT HOLD. NO PT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    144568 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8000

    Patients

    Seq Age Sex Outcome Treatment
    1