BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRUERESULT

    MDR report key: 4110733 · Received September 16, 2014

    Report

    Report Number
    1052693-2014-00319
    Event Type
    Malfunction
    Date Received
    September 16, 2014
    Date of Event
    August 17, 2014
    Report Date
    September 16, 2014
    Manufacturer
    NIPRO DIAGNOSTICS INC.
    Product Code
    NBW
    PMA / PMN Number
    K080641
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    PRODUCT NOT YET RETURNED FOR EVALUATION. INTERNAL REPORT NUMBER (B)(4). MANUFACTURER ACKNOWLEDGES LATENESS OF THE REPORT, PER INTERNAL CORRECTIVE ACTION. THIS REPORT SHOULD HAVE BEEN IDENTIFIED AS REPORTABLE WITHIN 30 DAYS OF THE IDENTIFICATION ((B)(4) 2014).

    Description of Event or Problem · 1

    CONSUMER COMPLAINT OF BLOOD RESULT READING OF "HI." LAST 5 BLOOD RESULTS IN MEMORY: HI, HI, 177 MG/DL, 277 MG/DL, 119 MG/DL. NO ADVERSE EVENT REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    572035 TRUERESULT BLOOD GLUCOSE SYSTEM NBW NIPRO DIAGNOSTICS INC. TRUERESULT PR1937

    Patients

    Seq Age Sex Outcome Treatment
    1