BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEARTSINE SAMARITAN 300P AND PAD PAK

    MDR report key: 3002170 · Received February 11, 2013

    Report

    Report Number
    3004123209-2013-00064
    Event Type
    Malfunction
    Date Received
    February 11, 2013
    Date of Event
    January 3, 2013
    Report Date
    January 23, 2013
    Manufacturer
    HEARTSINE TECHNOLOGIES, LTD
    Product Code
    MKJ
    PMA / PMN Number
    K052465
    Removal / Correction Number
    Z-0124-2013
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SP
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    ROUTINE TESTING CONFIRMED THAT THIS DEVICE WAS INSTALLED BY THE CUSTOMER IN (B)(6) 2011 AND THAT IT HAD PERFORMED TO SPEC TO UP THE RETURN OF THE DEVICE TO HEARTSINE ON (B)(6) 2013. THE INVESTIGATION CONFIRMED THAT THERE WAS A PROBLEM WHEN AN ATTEMPT WAS MADE TO UPGRADE THE SOFTWARE ON THE DEVICE TO VERSION 3.2.0 USING THE HEARTSINE UNIVERSAL UPGRADER. THIS DEVICE WAS REPLACED WITHIN 24 HOURS. THE PAD PAK, WHICH CONTAINS THE ELECTRODES AND BATTERIES, IS LABELLED FOR SINGLE USE BUT THE SAMARITAN PAD 300 AND 300P DEVICES ARE FOR MULTI-USE.

    Description of Event or Problem · 1

    THERE WAS NO PT INVOLVED IN THIS EVENT. THE DEVICE MALFUNCTIONED THAT THE SOFTWARE FAILED TO UPGRADE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    59542 HEARTSINE SAMARITAN 300P AND PAD PAK AUTOMATED EXTERNAL DEFIBRILLATOR MKJ HEARTSINE TECHNOLOGIES, LTD PAD

    Patients

    Seq Age Sex Outcome Treatment
    1