Retiro De Equipo (Recall) de Calibration Diskette and Assay Data Disks used with VITROS chemistry instruments. 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.

¿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
  • ID del evento
  • Clase de Riesgo del Evento
    Class II
  • Fecha de inicio del evento
  • País del evento
  • Fuente del evento
  • 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, inc. (ocd) has determined that the default dilution factors on the calibration diskette (cal disk) and assay data disks (add), drv 5740 and below, are incorrect. it has also been determined that the 2nd dilution factors contained in the engen laboratory automation system configuration (.Gsb) file (version 3.2.2 & below) are incorrect.
  • Acción
    Ortho-Clincial Diagnostics is providing their customers with Local Cal Disk or ADD version 5741 which contains the correct dilution factors. Customers are also advised to review their LIS data to determine the impact of the revised default dilution factors. For those customers using the enGen system, an Ortho-Clinical Diagnostics representative will assist in the development of revised dilution factors. This action has been closed-out on 12/02/2016.


  • Modelo / Serial
    Calibration Diskette and Assay Data Disks used with VITROS chemistry instruments. An in vitro diagnostic medical device (IVD)VITROS Chemistry Instruments: -VITROS 4600-VITROS 5600-VITROS 250-VITROS 350-VITROS 5,1 FS-enGen systemVITROS Chemistry Products:ALT slides -1655281 CK slides -8479396, -8478034LDH slides -8384489 hsCRP reagent -6801739 THC reagent -6801994 TIBC kit -8867541 METD reagent -6801996 CRBM slides -8892382
  • Manufacturer