BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ZOLL MEDICAL CORP

    MDR report key: 324638 · Received April 3, 2001

    Report

    Report Number
    324638
    Event Type
    Injury
    Date Received
    April 3, 2001
    Date of Event
    March 30, 2001
    Report Date
    April 3, 2001
    Manufacturer
    ZOLL MEDICAL CORP
    Product Code
    MKJ
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    LA, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    MONITOR WOULD NOT DEFIBRILLATE A PT IN CARDIOPULMONARY ARREST. MONITOR WOULD NOT DISPLAY "CHARGE AT 30 JOULES TO TEST." ANOTHER DEVICE AVAILABLE ON SCENE AND PT SUCCESSFULLY DEFIBRILLATED WITH THAT DEVICE USING THE SAME HANDS-FRR PADS ORIGINALLY APPLIED TO PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    14479 ZOLL MEDICAL CORP M SERIES MONITOR/DEFIBRILLATOR MKJ ZOLL MEDICAL CORP M SERIES NA

    Patients

    Seq Age Sex Outcome Treatment
    1 70 YR Life Threatening| R