BEUDAMED
    FDA Adverse Event Death Summary report: N

    ZOLL MEDICAL CORPORATION

    MDR report key: 170955 · Received June 3, 1998

    Report

    Report Number
    170955
    Event Type
    Death
    Date Received
    June 3, 1998
    Date of Event
    May 5, 1998
    Report Date
    May 26, 1998
    Manufacturer
    ZOLL MEDICAL CORP.
    Product Code
    LDD
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CODE WAS CALLED. DEFIBRILLATOR FAILED TO DISCHARGE. TWO REPORTS ARE BEING SUBMITTED ON THIS PT BECAUSE TWO DIFFERENT DEFIBRILLATORS FAILED TO DISCHARGE. THE OTHER DEFIBRILLATOR INVOLVED IN THIS INCIDENT WAS A ZOLL MODEL PD 1400.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZOLL MEDICAL CORPORATION PORTABLE CARDIAC DEFIBRILLATOR LDD ZOLL MEDICAL CORP. PD 1200 *

    Patients

    Seq Age Sex Outcome Treatment
    1 58 YR Death