BEUDAMED
    FDA Adverse Event Other Summary report: N

    CLINITEK STATUS

    MDR report key: 3190079 · Received June 20, 2013

    Report

    Report Number
    1217157-2013-00106
    Event Type
    Other
    Date Received
    June 20, 2013
    Date of Event
    June 11, 2013
    Report Date
    June 11, 2013
    Manufacturer
    SIEMENS HEALTHCARE DIAGNOSTICS INC.
    Product Code
    KQO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE CUSTOMER HAS BEEN RE-TRAINED FOR PROPER SAMPLING TECHNIQUE. CUSTOMER IS BEING PROVIDED WITH SOFTWARE THAT WILL GENERATE AN ERROR CODE (E50) ERROR INSTEAD OF MISIDENTIFYING THE STRIP.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THAT A MULTISTIX 10SG DIPSTICK READ ERRONEOUSLY AS A MULTISTIX PRO 10LB DIPSTICK ON THE INSTRUMENT. THERE WAS NO REPORT OF INJURY FOR THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    280925 CLINITEK STATUS CT STATUS KQO SIEMENS HEALTHCARE DIAGNOSTICS INC.

    Patients

    Seq Age Sex Outcome Treatment
    1