BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    M SERIES

    MDR report key: 288047 · Received July 27, 2000

    Report

    Report Number
    1220908-2000-00754
    Event Type
    Malfunction
    Date Received
    July 27, 2000
    Report Date
    June 26, 2000
    Manufacturer
    ZOLL MEDICAL CORPORATION
    Product Code
    KRF
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    COMPLAINANT ALLEGED THAT DURING ROUTINE TESTING, THE DEVICE DISPLAYED A "DEFIB FAULT 72". THERE WAS NO PT INVOLVEMENT DURING THE REPORTED MALFUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 M SERIES DEFIBRILLATOR/PACEMAKER KRF ZOLL MEDICAL CORPORATION MSERIES NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other