BEUDAMED
    FDA Adverse Event Death Summary report: N

    THUMPER

    MDR report key: 230071 · Received July 2, 1999

    Report

    Report Number
    1821850-1999-00004
    Event Type
    Death
    Date Received
    July 2, 1999
    Date of Event
    May 24, 1999
    Report Date
    July 2, 1999
    Manufacturer
    MICHIGAN INSTRUMENTS, INC.
    Product Code
    DRM
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    EMERGENCY MEDICAL TECHNICIAN

    Narratives

    Description of Event or Problem · 1

    THE USER REPORTED THAT AFTER APPLING THIS UNIT TO A PATIENT TO PERFORM CARDIOPULMONARY RESUSCITATION, IT WAS FOUND THAT THE UNIT WOULD NOT PERFORM COMPRESSIONS. AT THIS POINT THE UNIT WAS REMOVED FROM THE PATIENT AND MANUAL CPR WAS CONTINUED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 THUMPER CARDIOPULMONARY RESUSCITATOR DRM MICHIGAN INSTRUMENTS, INC. 1004 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN