BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COAGUCHEK ® XS SYSTEM

    MDR report key: 2942117 · Received February 4, 2013

    Report

    Report Number
    1823260-2013-00639
    Event Type
    Malfunction
    Date Received
    February 4, 2013
    Date of Event
    December 31, 2012
    Report Date
    March 20, 2013
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    GJS
    PMA / PMN Number
    K062925
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Additional Manufacturer Narrative · 1

    IT WAS UNKNOWN IF THE INITIAL REPORTER SENT REPORT TO THE FDA.

    Description of Event or Problem · 1

    CALLER STATES PATIENT TESTED 4.7 INR ON THE COAGUCHEK XS PLUS SYSTEM WHILE A COMPARISON LAB RETURNED AS 3.6 INR. PATIENT'S COUMADIN WAS ADJUSTED BASED ON THE REPORTED RESULTS. NO ADVERSE EVENT REPORTED. REQUESTED RETURN OF SUSPECT DEVICE AND REPLACEMENT WAS SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    47291 COAGUCHEK ® XS SYSTEM PROTHROMBIN TIME TEST STRIPS GJS ROCHE DIAGNOSTICS NA 21432911

    Patients

    Seq Age Sex Outcome Treatment
    1 035 YR COREG TWICE A DAY| MITRAL VALVE REPLACEMENT| LISINOPRIL DAILY| WARFARIN| POTASSIUM DAILY| FUROSEMIDE DAILY| AORTIC VALVE REPLACEMENT