BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEARTSTART MRX -EMS DEFIBRILLATOR

    MDR report key: 1894263 · Received November 3, 2010

    Report

    Report Number
    1218950-2010-02133
    Event Type
    Malfunction
    Date Received
    November 3, 2010
    Report Date
    October 5, 2010
    Manufacturer
    PHILIPS HEALTHCARE
    Product Code
    MKJ
    PMA / PMN Number
    K031187
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE CUSTOMER REPORTED THAT THE DEVICE WOULD NOT DELIVER A SHOCK DURING TESTING. THERE WAS NO REPORT OF PT IMPACT OR INVOLVEMENT. PHILIPS EVALUATED THE DEVICE AND REPLACED THE POWER PCA TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE DEVICE WOULD NOT DELIVER A SHOCK DURING TESTING. THERE WAS NO REPORT OF PT IMPACT OR INVOLVEMENT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1