BEUDAMED
    FDA Adverse Event Death Summary report: N

    CODEMASTER 100 PORTABLE DEFIBRILLATOR

    MDR report key: 215564 · Received March 10, 1999

    Report

    Report Number
    2425852-1999-00021
    Event Type
    Death
    Date Received
    March 10, 1999
    Date of Event
    January 25, 1999
    Report Date
    January 25, 1999
    Manufacturer
    HEWLETT-PACKARD CO.
    Product Code
    LDD
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DURING A CALL ON 1-25-99 INVOLVING A 67 YEAR OLD MALE PATIENT IN CARDIAC ARREST, THE UNIT WOULD NOT ALLOW THE CREW TO DEFIBRILLATE A PATIENT WHILE USING THE HANDS FREE CABLES AND 902400 PADS. THE FIRE DEPARTMENT ON THE SCENE WAS ABLE TO SHOCK THE PATIENT WITH THEIR AED. THE PATIENT CONVERTED TO A NON-TREATABLE RHYTHM AND WAS TRANSPORTED TO A HOSPITAL WHERE HE WAS PRONOUNCED. THE PADS WERE DISCARDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CODEMASTER 100 PORTABLE DEFIBRILLATOR SAED LDD HEWLETT-PACKARD CO. CM100 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Death