BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FREESTYLE

    MDR report key: 1061276 · Received June 19, 2008

    Report

    Report Number
    2954323-2007-06616
    Event Type
    Malfunction
    Date Received
    June 19, 2008
    Date of Event
    April 5, 2007
    Report Date
    May 4, 2007
    Manufacturer
    ABBOTT DIABETES CARE INC, USA
    Product Code
    LFR
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE METER HAS BEEN RETURNED AND AN INVESTIGATION IS IN PROCESS. CUSTOMERS AND RETAILERS HAVE BEEN INFORMED. INVESTIGATION IN PROCESS

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED AN ISSUE WITH THEIR METER WHICH SUGGESTS THE MEMORY OVERWRITE MALFUNCTION HAS OCCURED. THERE WAS NO REPORT OF DEATH OR SERIOUS INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FREESTYLE BLOOD GLUCOSE MONITORING SYSTEM LFR ABBOTT DIABETES CARE INC, USA NI 0627742

    Patients

    Seq Age Sex Outcome Treatment
    1