BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEARTSTART MRX

    MDR report key: 1972975 · Received January 20, 2011

    Report

    Report Number
    1218950-2011-00180
    Event Type
    Malfunction
    Date Received
    January 20, 2011
    Report Date
    December 24, 2010
    Manufacturer
    PHILIPS HEALTHCARE
    Product Code
    MKJ
    PMA / PMN Number
    K031187
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IT
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE CUSTOMER REPORTED THAT A THERAPY KNOB FAILURE WAS NOTED DURING OPCHECK, AND ORDERED A REPLACEMENT SWITCH TO RESOLVE THE ISSUE. THERE HAVE BEEN NO FURTHER CALLS RELATED TO THIS ISSUE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT A THERAPY KNOB FAILURE WAS NOTED DURING OPCHECK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEARTSTART MRX MKJ PHILIPS HEALTHCARE M3535A

    Patients

    Seq Age Sex Outcome Treatment
    1