BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ASCENSIA BREEZE2 TEST STRIPS (30)

    MDR report key: 1031913 · Received April 15, 2008

    Report

    Report Number
    1826988-2008-00402
    Event Type
    Malfunction
    Date Received
    April 15, 2008
    Date of Event
    March 24, 2008
    Report Date
    March 24, 2008
    Manufacturer
    BAYER HEALTHCARE LLC
    Product Code
    NBW
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER CALLED FOR HELP WITH HER NEW METER. WHILE PERFORMING CONTROL TESTS, SHE RECEIVED A RESULT OF "LO." THE NORMAL CONTROL RANGE WAS 89-121 MG/DL. NO ADVERSE EVENTS WERE ALLEGED. THE TEST STRIPS AND METER ARE TO BE RETURNED FOR EVAL. REPLACEMENT PRODUCTS WERE SENT TO THE CUSTOMER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ASCENSIA BREEZE2 TEST STRIPS (30) BLOOD GLUCOSE TEST STRIPS NBW BAYER HEALTHCARE LLC 866044 1A5131AA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK