BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    MDR report key: 1032680 · Received April 22, 2008

    Report

    Report Number
    1823260-2008-03414
    Event Type
    Malfunction
    Date Received
    April 22, 2008
    Date of Event
    March 23, 2008
    Report Date
    April 22, 2008
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K010362
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND

    Narratives

    Description of Event or Problem · 1

    REPORTER ALLEGED THAT COMFORT CURVE BLOOD GLUCOSE TEST STRIPS WERE LABELED WITH AN EXPIRATION DATE OF 01/31/09. THE MANUFACTURER'S BATCH RECORDS SHOW THE ACTUAL EXPIRATION DATE TO BE 01/31/08. NO ACTIONS OR TREATMENT WERE REPORTED IN CONNECTION WITH THE ALLEGED MALFUNCTION. NO ADVERSE EVENT REPORTED. A REQUEST WAS MADE FOR THE RETURN OF THE SUSPECT DEVICE AND REPLACEMENT PRODUCT 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 549502

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR COREG - 25MG TWICE DAILY| HUMALOG - 12ML DAILY| BENZONATATE - 100MG 3 TIMES DAILY| NORVASC - 10MG ONCE DAILY| CRESTOR - 10MG ONCE DAILY| "RENO CAP" - 800MG ONCE DAILY| LISINOPRIL - 10MG ONCE DAILY