BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FREESTYLE FLASH

    MDR report key: 811681 · Received January 16, 2007

    Report

    Report Number
    2954323-2007-00217
    Event Type
    Malfunction
    Date Received
    January 16, 2007
    Date of Event
    December 18, 2006
    Report Date
    January 16, 2007
    Manufacturer
    ABBOTT DIABETES CARE INC, USA
    Product Code
    LFR
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SW
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    COMPLAINT CONFIRMED. TESTED RETURNED UNIT. NO MANUFACTURING PARAMETERS FOUND OUT OF SPEC. UOM WAS SELECTABLE AND WAS RECEIVED AT MG/DL. ERRORS 015, 0204, 0300, 0800 AND 0806 WERE OBSERVED IN THE ERROR LOG INDICATING BATTERY DROOP. METER IS OPERABLE. CUSTOMERS AND RETAILERS HAVE BEEN INFORMED THROUGH THE FA16MAY2006 LETTER.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THE UNIT OF MEASURE SETTING OF THEIR UNLOCKED FREESTYLE FLASH METER CHANGED. 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 FLASH BLOOD GLUCOSE MONITORING SYSTEM LFR ABBOTT DIABETES CARE INC, USA NI NI

    Patients

    Seq Age Sex Outcome Treatment
    1 YR