BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANCE BED

    MDR report key: 3073010 · Received April 6, 2013

    Report

    Report Number
    1824206-2013-01954
    Event Type
    Malfunction
    Date Received
    April 6, 2013
    Date of Event
    March 7, 2013
    Report Date
    March 7, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE CUSTOMER TROUBLESHOT THE ISSUE DOWN TO THE TESTPORT CABLE AND REQUESTED REPLACEMENT. SEVERAL ATTEMPTS HAVE BEEN MADE TO ENSURE RESOLUTION; HOWEVER, NO OTHER INFORMATION HAS BEEN OBTAINED.

    Description of Event or Problem · 1

    CUSTOMER ALLEGED BED EXIT WOULD NOT ALARM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    141984 ADVANCE BED AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1105

    Patients

    Seq Age Sex Outcome Treatment
    1