BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COAGUCHEK XS SYSTEM

    MDR report key: 1063748 · Received June 19, 2008

    Report

    Report Number
    1823260-2008-04834
    Event Type
    Malfunction
    Date Received
    June 19, 2008
    Date of Event
    June 6, 2008
    Report Date
    June 19, 2008
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    GJS
    PMA / PMN Number
    K062925
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    CUSTOMER STATES THE PATIENT TESTED 4.4 INR ON THE COAGUCHEK XS SYSTEM AND 3.05 INR ON A COMPARISON LAB. NO ACTION TAKEN ON DEVICE RESULT. 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 20162831

    Patients

    Seq Age Sex Outcome Treatment
    1 41 YR CELEBREX - 200MG/DAY| COUMADIN - .5MG/DAY| VALIUM - 5MG/AS NEEDED| TAMOXIFEN CITRATE - 20MG/DAY| SENNA - 50MG/AS NEEDED| MIRALAX - 34G/DAY| DILAUDID - 2MG/AS NEEDED| ANCEF - 2G/8 HOURS| VITAMIN C| ABILIFY - 2MG/DAY| CALCIUM + D| FENTORA - 100MCG/AS NEEDED| FENTANYL LOLLIPOP - 200MCG/AS NEEDED| FENTANYL PATCH - 20MCG/DAY| ZOFRAN - 4MG/AS NEEDED| LORAZEPAM - 1MG/AS NEEDED| SALINE FLUSH - 2ML/IV| ZOMETA - 4MG/MONTHLY| LEXAPRO - 20MG/DAY