BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEART START XL

    MDR report key: 1851952 · Received September 23, 2010

    Report

    Report Number
    1218950-2010-01700
    Event Type
    Malfunction
    Date Received
    September 23, 2010
    Report Date
    August 26, 2010
    Manufacturer
    PHILIPS HEALTHCARE
    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). THE CUSTOMER REPORTED THAT THE DEVICE EXPERIENCED A "SYSTEM FAILURE, CYCLE POWER" MESSAGE. THERE WAS NO REPORT OF PATIENT INVOLVEMENT. THIS CUSTOMER REPORTED A FAILURE TO DISCHARGE DURING A PATIENT EVENT. THERE WAS NO IMPACT TO THE INVOLVED PATIENT.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE DEVICE EXPERIENCED A "SYSTEM FAILURE, CYCLE POWER" MESSAGE. THERE WAS NO REPORT OF 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