BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COAGUCHEK XS SYSTEM

    MDR report key: 1243235 · Received November 7, 2008

    Report

    Report Number
    1823260-2008-08242
    Event Type
    Malfunction
    Date Received
    November 7, 2008
    Date of Event
    October 31, 2008
    Report Date
    November 7, 2008
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    GJS
    PMA / PMN Number
    K062925
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    CALLER STATES THE PT TESTED 5.5 INR, 7.1 INR AND 5.3 INR ON THE COAGUCHEK XS SYSTEM DURING DUPLICATE TESTING. NO ACTION TAKEN ON DEVICE RESULTS. NO ADVERSE EVENT REPORTED. REQUESTED RETURN OF SUSPECT SYSTEM AND REPLACEMENT WAS SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COAGUCHEK XS SYSTEM PROTHROMBIN TIME TEST STRIPS, GJS GJS ROCHE DIAGNOSTICS 20163831

    Patients

    Seq Age Sex Outcome Treatment
    1 82 YR METFORMIN- NP 500MG/DAILY| LISIONPRIL- 20MG/DAY| ZOLPIDEM- 5MG/DAY| SIMVASTATIN- 30MG/DAY| OXYCODONE-5-325MG/ EVERY 6 HRS| PLAVIX- 75MG/DAY| COUMADIN- 3MG/3DAYS| LYRICA- 225MG/DAY| TRAMADOL HCL- 300MG/DAY| GLIPIZIDE- 5MG/DAY| HYDROCODONE APAP- 5-500MG/1-2 TABS EVERY 3 HRS| HYDROCHLOROTHIAZIDE- 25MG/DAY