BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CODEMASTER XL

    MDR report key: 3221521 · Received July 1, 2013

    Report

    Report Number
    1218950-2013-02754
    Event Type
    Malfunction
    Date Received
    July 1, 2013
    Report Date
    June 4, 2013
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    LDD
    PMA / PMN Number
    K954957
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IT
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). A FOLLOW UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE DEVICE IS NOT CHARGING THE BATTERY DESPITE BEING PLUGGED IN TO AC (MAINS) POWER. NO REPORT OF PATIENT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    297782 CODEMASTER XL MKJ, DQA LDD PHILIPS MEDICAL SYSTEMS M1723B

    Patients

    Seq Age Sex Outcome Treatment
    1