BEUDAMED
    FDA Adverse Event Other Summary report: N

    BD PARADIGM LINK GLUCOSE MONITOR

    MDR report key: 1060891 · Received June 13, 2008

    Report

    Report Number
    3004193489-2008-00467
    Event Type
    Other
    Date Received
    June 13, 2008
    Date of Event
    June 9, 2008
    Report Date
    June 13, 2008
    Manufacturer
    NOVA BIOMEDICAL CORP.
    Product Code
    NBW
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    NOVA BIOMEDICAL AWAITS THE RETURN OF THE DEVICE FOR EVALUATION. SHOULD ANY SIGNIFICANT FINDINGS BE A RESULT OF THAT INVESTIGATION, A FOLLOW-UP REPORT WILL BE FILED.

    Description of Event or Problem · 1

    IT WAS REPORTED TO NOVA BIOMEDICAL THAT A CONSUMER EXPERIENCED A HYPOGLYCEMIC EVENT REQUIRING MEDICAL INTERVENTION. ACCORDING TO THE CONSUMER'S SPOUSE, "I TREATED HIM BASED ON A READING AND HAD TO GO TO THE HOSPITAL BECAUSE OF A REACTION." THE CONSUMER'S SPOUSE DECLINED TO PROVIDE ANY INFORMATION REGARDING THIS ADVERSE EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD PARADIGM LINK GLUCOSE MONITOR GLUCOSE MONITOR NBW NOVA BIOMEDICAL CORP. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK