BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CODEMASTER XL + DEFIBRILLATOR

    MDR report key: 4250494 · Received November 7, 2014

    Report

    Report Number
    1218950-2014-06742
    Event Type
    Malfunction
    Date Received
    November 7, 2014
    Report Date
    October 13, 2014
    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).

    Description of Event or Problem · 1

    IT WAS REPORTED TO PHILIPS THAT THE HEARTSTART CODEMASTER XL + DEFIBRILLATOR DID NOT PASS THE DAILY INITIAL TEST. THERE WAS NO PATIENT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    718740 CODEMASTER XL + DEFIBRILLATOR LDD, MKJ, DQA LDD PHILIPS MEDICAL SYSTEMS M1722A

    Patients

    Seq Age Sex Outcome Treatment
    1