BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COAGUCHEK® XS SYSTEM

    MDR report key: 1940389 · Received December 29, 2010

    Report

    Report Number
    1823260-2010-07709
    Event Type
    Malfunction
    Date Received
    December 29, 2010
    Date of Event
    December 20, 2010
    Report Date
    February 8, 2011
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    GJS
    PMA / PMN Number
    K062925
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    DE, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    CALLER STATES SHE TESTED 6.5 INR AND 3.4 INR ON THE COAGUCHEK XS SYSTEM. NO ACTIONS WERE REPORTED TAKEN OR TREATMENT RECEIVED. NO ADVERSE EVENT REPORTED. A REQUEST WAS MADE FOR THE RETURN OF THE AFFECTED PRODUCT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COAGUCHEK® XS SYSTEM PROTHROMBIN TIME TEST STRIPS GJS ROCHE DIAGNOSTICS NA 20182128

    Patients

    Seq Age Sex Outcome Treatment
    1 069 YR COUMADIN| MAXZIDE| REPLACEMENT HEART VALVE| CALCIUM| LISINOPRIL| NORVASC| ZETIA