BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FREESTYLE FREEDOM

    MDR report key: 1030266 · Received April 17, 2008

    Report

    Report Number
    2954323-2008-01503
    Event Type
    Injury
    Date Received
    April 17, 2008
    Date of Event
    March 19, 2008
    Report Date
    April 17, 2008
    Manufacturer
    ABBOTT DIABETES CARE INC, USA
    Product Code
    LFR
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS IS AN INITIAL REPORT. THE CUSTOMER'S PRODUCT HAS BEEN REQUESTED BACK FOR AN INVESTIGATION. A FOLLOW-UP REPORT WILL BE FILED ONCE INVESTIGATION RESULTS ARE AVAILABLE.

    Description of Event or Problem · 1

    CUSTOMER'S FAMILY MEMBER REPORTED CUSTOMER SELF TREATED WITH INSULIN BASED ON THE READINGS OBTAINED FROM THEIR FREESTYLE FREEDOM METER AND LOST CONSCIOUSNESS SHORTLY AFTER THAT. PARAMEDICS WERE CALLED AND PLACED CUSTOMER ON UNKNOWN IV SOLUTION. CUSTOMER WAS THEN TAKEN TO HOSPITAL. THERE IS NO REPORT OF ANY DIAGNOSIS, AN INVESTIGATION INTO THE DETAILS OF THIS EVENT IS IN PROCESS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FREESTYLE FREEDOM BLOOD GLUCOSE MONITORING SYSTEM LFR ABBOTT DIABETES CARE INC, USA NA 0729829

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Hospitalization| R