Retiro De Equipo (Recall) de VITROS Chemistry Products Calibrator Kit 25 (used on VITROS 4600/5600 Systems and with VITROS Chemistry Products dHDL Slides). An in vitro diagnostic medical device (IVD).

Según Department of Health, Therapeutic Goods Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Australia que fue producido por Ortho-Clinical Diagnostics Australia Pty Ltd.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • ID del evento
    RC-2016-RN-01376-1
  • Clase de Riesgo del Evento
    Class III
  • Fecha de inicio del evento
    2016-10-18
  • País del evento
  • Fuente del evento
    DHTGA
  • URL de la fuente del evento
  • Notas / Alertas
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Australia.
  • Notas adicionales en la data
  • Causa
    Ortho clinical diagnostics has confirmed that some barcode labels included in some vitros calibrator kit 25, lot 2576 cartons contain an incorrect lot number. the labels indicate lot 2575 instead of the correct lot 2576 for all three calibrator levels. the printed barcode labels are used with the automatic calibration feature when calibrating vitros 4600 or 5600 systems. when the operator attempts to use the affected barcode labels to calibrate vitros dhdl slides, a ‘pzc-006’ condition code occurs, indicating that the calibrator lot is not supported by the assay data disk (add); therefore the calibration is not successful. all labelling on the calibrator vials and the carton is correct. lot 2576 calibrators perform as expected if the operator manually programs the correct lot information for calibration.
  • Acción
    Ortho is advising users to inspect the barcode labels provided in VITROS Calibrator Kit 25, Lot 2576, discard affected labels that indicate Lot 2575, and to manually program Lot 2576 when calibrating VITROS dHDL Slides.

Device

  • Modelo / Serial
    VITROS Chemistry Products Calibrator Kit 25 (used on VITROS 4600/5600 Systems and with VITROS Chemistry Products dHDL Slides). An in vitro diagnostic medical device (IVD).Product Code: 6801896Lot Number: 2576Expiry Date: 02 Sept 2017ARTG Number: 232248
  • Manufacturer

Manufacturer