BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEARTSTART MRX-EMS DEFIBRILLATOR

    MDR report key: 1214050 · Received October 23, 2008

    Report

    Report Number
    1218950-2008-00573
    Event Type
    Malfunction
    Date Received
    October 23, 2008
    Report Date
    September 23, 2008
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE CUSTOMER REPORTED THAT THIS UNIT HAD A RED X AFTER PUTTING A BATTERY IN. THE UNIT WAS EVALUATED AT THE CUSTOMER SITE BY A PHILIPS FIELD SUPPORT ENGINEER. THE BATTERY PCA WAS REPLACED WHICH RESOLVED THIS ISSUE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THIS UNIT HAD A RED X AFTER PUTTING A BATTERY IN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEARTSTART MRX-EMS DEFIBRILLATOR DEFIBRILLATOR LDD PHILIPS MEDICAL SYSTEMS M3536A

    Patients

    Seq Age Sex Outcome Treatment
    1