BEUDAMED
    FDA Adverse Event Summary report: N

    ZOLL SMART BATTERY

    MDR report key: 1183064 · Received August 7, 2008

    Report

    Report Number
    1183064
    Date Received
    August 7, 2008
    Date of Event
    August 7, 2008
    Report Date
    August 7, 2008
    Manufacturer
    ZOLL MEDICAL CORPORATION
    Product Code
    MOQ
    Report Source
    User Facility report
    Reporter Location
    RI, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    ZOLL BATTERY READ OVER CHARGE REMOVED-BATTERY AND HOT LIQUID POURED OUT THE END ONTO THE NURSE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZOLL SMART BATTERY BATTERY, DEFIBRILLATOR MOQ ZOLL MEDICAL CORPORATION NOT KNOWN NOT KNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 *