BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEWLETT PACKARD CO

    MDR report key: 79150 · Received February 12, 1997

    Report

    Report Number
    79150
    Event Type
    Malfunction
    Date Received
    February 12, 1997
    Date of Event
    December 5, 1996
    Report Date
    December 18, 1996
    Manufacturer
    HEWLETT PACKARD
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    OK, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    INTERNAL DEFIBRILLATOR PADDLES WERE BEING USED DURING OPEN HEART SURGERY. WHEN THE DEFIBRILLATOR WAS CHARGED, IT IMMEDIATELY DISCHARGED, BEFORE THE CABLE PADDLE DISCHARGE SWITCH WAS DEPRESSED. A SECOND SET OF CABLES WAS INSTALLED AND OPERATED PROPERLY. NO PT INJURY OCCURRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEWLETT PACKARD CO INTERNAL DEFIBRILLATOR PADDLE CABLE LDD HEWLETT PACKARD 149909-931101 *

    Patients

    Seq Age Sex Outcome Treatment
    1 59 YR Other