Events

Retiro De Equipo (Recall) de ADVIA Chemistry XPT System with software versions 1.0.3 and 1.1. 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 Siemens Healthcare 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-00569-1
  • Clase de Riesgo del Evento
    Class II
  • Fecha de inicio del evento
    2016-05-03
  • País del evento
    Australia
  • Fuente del evento
    DHTGA
  • URL de la fuente del evento
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2016-RN-00569-1
  • 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
    Siemens has identified multiple software issues that may affect the day-to-day behaviour and/or workflow of the system.1. all levels of qc run when only 1 is selected in start/restart window 2. changing the display name of an assay deselects that method in its associated qc panel, therefore qc for the renamed assay will not run as part of the panel. 3. a workstation services restart screen may appear under multiple scenarios, causing the user interface to be temporarily inaccessible. the user will be prompted to login once the services restart. a.Workstation services may restart if a user defined filter is created in the test results overview screen that includes the 31st day of the month, but is run in a month that does not have 31 days. b.Workstation services may also restart when all items are removed from the watchlist. 4. the chemistry xpt software does not update assay utilisation counters for ise tests when patient samples and qc samples are run in version v1.1.
  • Acción
    Siemens is providing users with work around instructions to follow as an interim measure. A software upgrade will be installed as a permanent correction. Users are advised to review the issues with the Medical Director.

Device

ADVIA Chemistry XPT System with software versions 1.0.3 and 1.1. An in vitro diagnostic medical d...
  • Modelo / Serial
    ADVIA Chemistry XPT System with software versions 1.0.3 and 1.1. An in vitro diagnostic medical device (IVD)Siemens Material Number (SMN): 10723034ARTG Number: 175890
  • Manufacturer
    Siemens Healthcare Pty Ltd

Manufacturer

Siemens Healthcare Pty Ltd
  • Empresa matriz del fabricante (2017)
    Siemens AG
  • Source
    DHTGA