BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    WATER RESISTANT EXTERNAL PADDLES

    MDR report key: 2920905 · Received December 26, 2012

    Report

    Report Number
    1218950-2012-04235
    Event Type
    Malfunction
    Date Received
    December 26, 2012
    Report Date
    November 28, 2012
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    MKJ
    PMA / PMN Number
    K031187
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IT
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4): THE CUSTOMER REPORTED THAT THE DEFIBRILLATOR PLATE WAS BROKEN. THERE WAS NO REPORTED PT INVOLVEMENT. THIS COMPLAINT IS STILL BEING INVESTIGATED. A F/U REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE DEFIBRILLATOR PLATE WAS BROKEN. THERE WAS NO REPORTED PT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 WATER RESISTANT EXTERNAL PADDLES MKJ PHILIPS MEDICAL SYSTEMS M3543A

    Patients

    Seq Age Sex Outcome Treatment
    1