BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEART START XL

    MDR report key: 1905607 · Received November 11, 2010

    Report

    Report Number
    1218950-2010-02236
    Event Type
    Malfunction
    Date Received
    November 11, 2010
    Report Date
    October 13, 2010
    Manufacturer
    PHILIPS HEALTHCARE
    Product Code
    MKJ
    PMA / PMN Number
    K001725
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SP
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4): THE CUSTOMER REPORTED THAT THE BATTERY FAILED TO STAY INSERTED. THERE WAS NO REPORT OF PT INVOLVEMENT. THE UNIT WAS EVALUATED LOCALLY BY PHILIPS AND THE FAILURE WAS VERIFIED. REPLACING THE BATTERY LATCH RESOLVED THE FAILURE. THE UNIT PASSED ALL POST-SERVICING TESTING AND REMAINS AT THE CUSTOMER SITE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE BATTERY FAILED TO STAY INSERTED. THERE WAS NO REPORT OF PT 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