BEUDAMED
    FDA Adverse Event Summary report: N

    MEGA 2000

    MDR report key: 1734488 · Received June 18, 2010

    Report

    Report Number
    1734488
    Date Received
    June 18, 2010
    Date of Event
    October 4, 2009
    Report Date
    December 30, 2009
    Manufacturer
    MEGADYNE MEDICAL PRODUCTS INC
    Product Code
    GEI
    Report Source
    User Facility report
    Reporter Location
    IL, US

    Narratives

    Description of Event or Problem · 1

    THE CAUTERY DIDN'T WORK WHEN PT WAS HAVING AN UNSCHEDULED C-SECTION. STAFF REPLACED THE ELECTROSURGICAL PATIENT RETURN ELECTRODE PAD AND THE CAUTERY WORKED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEGA 2000 PATIENT RETURN ELECTRODE GEI MEGADYNE MEDICAL PRODUCTS INC MEGA 2000 *

    Patients

    Seq Age Sex Outcome Treatment
    1 26 YR NONE KNOWN