BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DURASTAR STRETCHER

    MDR report key: 2922683 · Received December 27, 2012

    Report

    Report Number
    1824206-2012-08648
    Event Type
    Malfunction
    Date Received
    December 27, 2012
    Date of Event
    December 12, 2012
    Report Date
    December 12, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE REPAIR IS NOT COMPLETED. A F/U REPORT WILL BE SENT ONCE THE REPAIR IS COMPLETE.

    Description of Event or Problem · 1

    THE COMPLAINANT STATED THAT THE RIGHT SIDERAIL WILL NOT LATCH AND REMAIN IN THE LATCHED POSITION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DURASTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8005

    Patients

    Seq Age Sex Outcome Treatment
    1