BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEARTSTART MRX - EMS DEFIBRILLATOR

    MDR report key: 1961487 · Received January 10, 2011

    Report

    Report Number
    1218950-2011-00076
    Event Type
    Malfunction
    Date Received
    January 10, 2011
    Report Date
    December 13, 2010
    Manufacturer
    PHILIPS HEALTHCARE
    Product Code
    MKJ
    PMA / PMN Number
    K031187
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4): THE CUSTOMER REPORTED 12-LEAD ECG SIGNAL LOSS. THERE WAS NO REPORT OF PT IMPACT. A PHILIPS FIELD SERVICE ENGINEER REPORTED HAVING EVALUATED THE DEVICE, CONFIRMED THE ISSUE, AND RESOLVED THE ISSUE BY REPLACING THE LEAD'S ECG TRUNK CABLE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED 12-LEAD ECG SIGNAL LOSS. THERE WAS NO REPORT OF PT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEARTSTART MRX - EMS DEFIBRILLATOR MKJ PHILIPS HEALTHCARE M3536A 7D

    Patients

    Seq Age Sex Outcome Treatment
    1