BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEARTSTREAM FR2

    MDR report key: 2191047 · Received July 25, 2011

    Report

    Report Number
    3030677-2011-00110
    Event Type
    Malfunction
    Date Received
    July 25, 2011
    Report Date
    July 13, 2011
    Manufacturer
    PHILIPS MEDICAL SYSTEMS (HTST)
    Product Code
    MKJ
    PMA / PMN Number
    003565
    Removal / Correction Number
    Z-0470/0473-2011
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    HK
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). CURRENTLY PENDING DEVICE EVAL.

    Description of Event or Problem · 1

    AED IS PART OF A RECALL POPULATION AND ALSO AS AN ASSOCIATED COMPLAINT. THE REPORTED FAILURE IS NOT INDICATIVE OF THE RECALLED COMPONENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEARTSTREAM FR2 MKJ PHILIPS MEDICAL SYSTEMS (HTST) M3840A

    Patients

    Seq Age Sex Outcome Treatment
    1