BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    MDR report key: 1053173 · Received May 27, 2008

    Report

    Report Number
    1823260-2008-04318
    Event Type
    Malfunction
    Date Received
    May 27, 2008
    Date of Event
    May 13, 2008
    Report Date
    May 27, 2008
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K010362
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CALLER REPORTS BACK TO BACK COMPARISON OF METER TO LAB WHILE USING THE INFORM SYSTEM WITH RESULTS OF 564MG/DL ON THE METER AND 145MG/DL AT THE LAB. OTHER METER TO METER COMPARISON NOTED; INVALID DUE TO A VALID METER TO LAB COMPARISON. CALLER REPORTS CONTROLS WERE RUN AND PASSED. NO ADVERSE EVENT REPORTED. A REQUEST WAS MADE FOR RETURN OF THE SUSPECT PRODUCT AND A REPLACEMENT WAS SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK COMFORT CURVE TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS - LFR LFR ROCHE DIAGNOSTICS 550608

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK