BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COAGUCHEK® XS SYSTEM

    MDR report key: 1930065 · Received December 16, 2010

    Report

    Report Number
    1823260-2010-07497
    Event Type
    Malfunction
    Date Received
    December 16, 2010
    Date of Event
    November 27, 2010
    Report Date
    January 10, 2011
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    GJS
    PMA / PMN Number
    K062925
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UT, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CALLER STATES THE PATIENT TESTED 2.9 INR ON THE COAGUCHEK XS SYSTEM AND >10.0INR ON A COMPARISON HOSPITAL 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 20182131

    Patients

    Seq Age Sex Outcome Treatment
    1 030 YR POTASSIUM| KLONOPIN| COLACE| LYRICA| "ARGINAIDE PROTEIN SUPPLEMENT"| COUMADIN (DAILY)| SENNA| MUCINEX (AS NEEDED)| MAGNESIUM| CALCIUM/VITAMIN D (DAILY)| ZINC SULFATE| VITAMIN C| FERROUS SULFATE| VALIUM| TRAZODONE| SEROQUEL| SKELAXIN| METOPROLOL| CELEXA| OXYCONTIN| NAPROXEN| PHENERGAN| FOSAMAX| PROTONIX