BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEART START XL

    MDR report key: 2241462 · Received August 9, 2011

    Report

    Report Number
    1218950-2011-02321
    Event Type
    Malfunction
    Date Received
    August 9, 2011
    Report Date
    July 14, 2011
    Manufacturer
    AGILENT TECHNOLOGIES, INC
    Product Code
    MKJ
    PMA / PMN Number
    K001725
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CH
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THIS CUSTOMER REPORTED A FAILURE TO DISCHARGE. THERE WAS NO REPORT OF ANY PT INVOLVEMENT. THIS COMPLAINT IS STILL BEING INVESTIGATED. A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

    Description of Event or Problem · 1

    THIS CUSTOMER REPORTED A FAILURE TO DISCHARGE. THERE WAS NO REPORT OF ANY PT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEART START XL MKJ AGILENT TECHNOLOGIES, INC M4735A

    Patients

    Seq Age Sex Outcome Treatment
    1