BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEARTSTAREAM FR2

    MDR report key: 2901420 · Received January 2, 2013

    Report

    Report Number
    3030677-2013-00001
    Event Type
    Malfunction
    Date Received
    January 2, 2013
    Report Date
    December 20, 2012
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    MKJ
    PMA / PMN Number
    003565
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). PRODUCT EVALUATION PENDING. ISSUE IS BEING REPORTED AS ALERT COULD NOT BE CLEARED BY OPERATOR.

    Description of Event or Problem · 1

    IT HAS BEEN REPORTED THAT THE AED DID NOT PASS SELF DIAGNOSTIC CHECK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    374 HEARTSTAREAM FR2 MKJ PHILIPS MEDICAL SYSTEMS M3840A

    Patients

    Seq Age Sex Outcome Treatment
    1