BEUDAMED
    FDA Adverse Event Other Summary report: N

    LIFEPAK

    MDR report key: 404283 · Received July 10, 2002

    Report

    Report Number
    MW1025502
    Event Type
    Other
    Date Received
    July 10, 2002
    Date of Event
    June 28, 2002
    Report Date
    July 8, 2002
    Manufacturer
    PHYSIO-CONTROL
    Product Code
    LDD
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    DEFIBRILLATOR DISCHARGED WHILE STILL CHARGING. MD WAS PERFORMING COMPRESSIONS AND ALSO RECEIVED A SHOCK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIFEPAK 9P DEFIBRILLATOR LDD PHYSIO-CONTROL 9P NA

    Patients

    Seq Age Sex Outcome Treatment
    1 74 YR Other