BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANTA

    MDR report key: 1070834 · Received July 3, 2008

    Report

    Report Number
    1824206-2008-02781
    Event Type
    Malfunction
    Date Received
    July 3, 2008
    Date of Event
    June 9, 2008
    Report Date
    June 9, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    WHEN THE HEAD IS FULLY RAISED, THE HILOW WILL NOT LOWER. AS A RESULT THE REVERSE TRENDELENBURG WAS NOT WORKING ON THIS BED. A HILL-ROM TECH REPLACED THE HEAD HILOW LIMIT SWITCH TO RESOLVE THE ISSUE. THE HEAD HILOW LIMIT SWITCH THAT WAS REMOVED WAS SCRAPPED. NO INJURIES REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ADVANTA AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1600 N/A

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK