BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRUERESULT

    MDR report key: 3980299 · Received June 5, 2014

    Report

    Report Number
    1052693-2014-00153
    Event Type
    Malfunction
    Date Received
    June 5, 2014
    Date of Event
    May 3, 2014
    Report Date
    June 5, 2014
    Manufacturer
    NIPRO DIAGNOSTICS, INC.
    Product Code
    LFR
    PMA / PMN Number
    K080641
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VT, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    PRODUCT NOT YET RETURNED FOR EVALUATION. (B)(4). THE MFR ACKNOWLEDGES THE LATENESS OF THIS REPORT.

    Description of Event or Problem · 1

    CONSUMER COMPLAINT OF SOME TEST STRIPS READING "LO" BLOOD RESULTS. NO ADVERSE EVENT REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    329910 TRUERESULT BLOOD GLUCOSE SYS LFR NIPRO DIAGNOSTICS, INC. TRUERESULT PP1163

    Patients

    Seq Age Sex Outcome Treatment
    1