BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    6000CMS IOD

    MDR report key: 3173043 · Received May 30, 2013

    Report

    Report Number
    1722139-2013-01341
    Event Type
    Malfunction
    Date Received
    May 30, 2013
    Date of Event
    September 8, 2011
    Report Date
    December 12, 2011
    Manufacturer
    MOOG DEVICE GROUP
    Product Code
    FRN
    PMA / PMN Number
    K981816
    Removal / Correction Number
    Z-1868-2011
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION FOUND THAT PUMP HAD EXPERIENCED ERROR CODE 45 IN PUMP'S HISTORY. NEW PUMP SOFTWARE WAS INSTALLED. (B)(4).

    Description of Event or Problem · 1

    INFO RECEIVED STATES THAT PUMP HAD EXPERIENCED ERROR CODE 45.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    238707 6000CMS IOD FRN MOOG DEVICE GROUP 6000CMS IOD

    Patients

    Seq Age Sex Outcome Treatment
    1