BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ZOLL MEDICAL CORPORATION

    MDR report key: 475389 · Received July 30, 2003

    Report

    Report Number
    475389
    Event Type
    Injury
    Date Received
    July 30, 2003
    Date of Event
    July 15, 2003
    Report Date
    July 23, 2003
    Manufacturer
    ZOLL MEDICAL CORPORATION
    Product Code
    MKJ
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    NE, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ENERGY SELECT BUTTON DOES NOT FUNCTION PROPERLY WHEN LOWERING JOULES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZOLL MEDICAL CORPORATION DEFIBRILLATOR -M-SERIES MKJ ZOLL MEDICAL CORPORATION * *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention