BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FR2

    MDR report key: 1791437 · Received August 6, 2010

    Report

    Report Number
    3030677-2010-00269
    Event Type
    Malfunction
    Date Received
    August 6, 2010
    Report Date
    August 6, 2010
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    MKJ
    PMA / PMN Number
    003565
    Removal / Correction Number
    Z-00063-2010
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE 510(K) IS FOR FIRST FR2 CLEARANCE. METHOD: DEVICE INTERNAL MEMORY REVIEWED.

    Description of Event or Problem · 1

    DEVICE DISPLAYED AN ERROR CODE THAT WAS SUBJECT TO SUBSEQUENT FIELD ACTION (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FR2 AED MKJ PHILIPS MEDICAL SYSTEMS M3841A-ABU

    Patients

    Seq Age Sex Outcome Treatment
    1