BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FREESTYLE

    MDR report key: 1800608 · Received September 7, 2007

    Report

    Report Number
    2954323-2007-16675
    Event Type
    Malfunction
    Date Received
    September 7, 2007
    Date of Event
    August 9, 2007
    Report Date
    September 7, 2007
    Manufacturer
    ABBOTT DIABETES CARE INC., USA
    Product Code
    NBW
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE DEVICE (V-G177- (B)(4)) AND STRIPS (B)(4) WERE RETURNED. THE COMPLAINT WAS NOT CONFIRMED AND NO NEW ISSUES WERE OBSERVED DURING PRODUCT TESTING. ALL RESULTS WERE WITHIN THE RANGE SPECIFICATION AND NO ERRORS OR OBSERVED DURING CONTROL SOLUTION TESTING. THE READINGS REPORTED BY THE CUSTOMER ARE PRESENT IN THE METER'S MEMORY LOG.

    Description of Event or Problem · 1

    CUSTOMER REPORTED RECEIVING ERRATIC READINGS ON THEIR FREESTYLE BLOOD GLUCOSE MONITOR. CUSTOMER REPORTED RECEIVING READINGS OF 156 MG/DL AND A "HI" MESSAGE (A "HI" INDICATES A READING GREATER THAN 500 MG/DL) WITHIN 10 MINUTES. ALL TESTS WERE PERFORMED ON THE FINGER. THE RESULTS WHEN PLOTTED ON A PARKES ERROR GRID FELL INTO THE "C" ZONE SHOWING THE DIFFERENCE IN VALUES TO BE CLINICALLY SIGNIFICANT. THERE WAS NO REPORT OF DEATH, SERIOUS INJURY OR MISTREATMENT ASSOCIATED WITH THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FREESTYLE BLOOD GLUCOSE MONITORING SYSTEM NBW ABBOTT DIABETES CARE INC., USA NI 0707503

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK