Retiro De Equipo (Recall) de Sysmex XN-9000 Automated Haematology System. 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 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
  • 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
    A remote possibility exists of incorrect allocation of customer demographic information against a sample in a specific situation. in a situation where the patient demographic information for a sample is not entered at the host computer and if the sample position is manually changed after being read by the barcode terminal, the customer demographics may be incorrectly allocated to the wrong patient results. one complaint worldwide has been received for this issue and in this instance, the user was not following the instructions for use, which clearly indicate that tubes should neither be removed nor inserted from the tube rack after a sample processing run has started. however, a software issue has also been identified with this system.
  • Acción
    Sysmex is preparing a software patch for mandatory upgrade, which Roche Diagnostics’ personnel will install on the affected systems (software expected by end January 2017). Roche Diagnostics Australia will contact customers to arrange the install. In the interim, users are to ensure that: - They do not remove a rack in transit, or insert a rack or sample in anything other than the feeder when analysis is in progress; - If a STAT sample needs to be processed, they perform a manual analysis or off-line analysis; - If any sample results are sent to “Pending”, they perform a delta check; - Patient information is entered at the host computer and use both sample and patient ID. This action has been closed-out on 01/03/2018.


  • Modelo / Serial
    Sysmex XN-9000 Automated Haematology System. An in vitro diagnostic medical device (IVD).Product Name/Code: XN-9000 Supply Parts AE415692Roche Material Number: 06509908001All Serial NumbersARTG Number: 173886
  • Manufacturer