BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ZOLL MEDICAL CORP

    MDR report key: 1723888 · Received June 14, 2010

    Report

    Report Number
    1723888
    Event Type
    Malfunction
    Date Received
    June 14, 2010
    Date of Event
    June 3, 2010
    Report Date
    June 8, 2010
    Manufacturer
    ZOLL
    Product Code
    MLN
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE DEFIBRILLATION ELECTRODES HAD A SHORT WHICH CAUSED THE DEFIBRILLATOR FROM DELIVERING A SHOCK AND UNABLE TO DISABLE THE SYNC.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZOLL MEDICAL CORP ONESTEP COMPLETE ELECTRODE MLN ZOLL 09456714 5209

    Patients

    Seq Age Sex Outcome Treatment
    1 66 YR