Retiro De Equipo (Recall) de Sysmex XN and XN-L Series - All Sysmex XN analysers versions 16 to 19

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

¿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-2015-RN-01165-1
  • Clase de Riesgo del Evento
    Class III
  • Fecha de inicio del evento
    2015-12-09
  • 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
    Roche diagnostics has been informed by sysmex that incorrect data transfer to the host computer may sporadically occur, when using the sysmex xn analysers, versions 16 to 19. this may lead to delays in reporting results and false negative results. under certain situations data may not be sent to the host computer, or incorrect data may be transferred. an example of incorrect data transfer may be if data is transferred as wbc, rbc, aso%, neut# and if this occurs at the transfer of baso% data, then all of the subsequent item’s data will be overwritten as baso% data. it has not yet been established which item overwrites the subsequent item’s data. if multiple samples were selected, and those selected samples were sent to the host computer as batch data, then this issue may be observed on multiple samples.
  • Acción
    Roche Diagnostics will perform a software update on the affected devices. Roche is advising the users to investigate result transmission for data integrity if the error messages “TCP/IP send error occurred at host computer” or “Unable to establish TCP/IP connection with host computer” have been noticed prior to the software patch being installed. This action has been closed-out on 05/09/2016.

Device

Manufacturer