BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2922989 · Received December 27, 2012

    Report

    Report Number
    1824206-2012-08601
    Event Type
    Malfunction
    Date Received
    December 27, 2012
    Date of Event
    December 11, 2012
    Report Date
    December 11, 2012
    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

    THE TECHNICIAN ISOLATED THE ISSUE TO A BROKEN ROCKER ARM. HE INSTALLED A BRAKE/STEER UPGRADE KIT TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE BRAKE OR STEER WILL NOT SET FROM FOOT END. THE BRAKE/STEER CAN BE SET FROM THE HEAD END AND THE STRETCHER WOULD APPEAR TO BE IN BRAKE MODE BUT THE FOOT END CASTER WOULD NOT ENGAGE (HOLD).

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1