BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEART START XL

    MDR report key: 2050540 · Received April 5, 2011

    Report

    Report Number
    1218950-2011-00920
    Event Type
    Malfunction
    Date Received
    April 5, 2011
    Report Date
    March 10, 2011
    Manufacturer
    PHILIPS HEALTHCARE
    Product Code
    MKJ
    PMA / PMN Number
    K001725
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4): THE CUSTOMER REPORTED RECURRING EXTENDED SELF TEST ERROR CODE 90007 PACER FAILURE. THERE WAS NO PATIENT INVOLVEMENT. THIS REPORT IS CANCELLED BECAUSE CURRENTLY MDR IS BEING USED IN PLACE OF THE SPECIFIC REGION REPORT.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED RECURRING EXTENDED SELF TEST ERROR CODE 90007 PACER FAILURE. THERE WAS NO PATIENT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEART START XL MKJ PHILIPS HEALTHCARE M4735A

    Patients

    Seq Age Sex Outcome Treatment
    1