Events

Retiro De Equipo (Recall) de Artis Zeego systems (Angiographic fluoroscopic digital diagnostic x-ray system) with software Artis VC20x/VC21A/VD10x that have a DSA license installed

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 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-2013-RN-00212-1
  • Clase de Riesgo del Evento
    Class I
  • Fecha de inicio del evento
    2013-03-08
  • 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-2013-RN-00212-1
  • 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
    There is a potential issue on artis systems with the software artis vc20x/vc21a/vd10x that have a dsa license installed. under certain preconditions, executing roadmap ogp (organ program) in the dsa overlay mode may lead to imprecise overlay of the dsa mask image with the roadmap image displayed on the live monitor.
  • Acción
    End users are being requested to keep the system (stand or table) stationary between DSA taken and DSA used as mask when executing the OGP roadmap in the DSA overlay mode. A software update will be implemented to correct the issue.

Device

Artis Zeego systems (Angiographic fluoroscopic digital diagnostic x-ray system) with software Art...
  • Modelo / Serial
    Artis Zeego systems (Angiographic fluoroscopic digital diagnostic x-ray system) with software Artis VC20x/VC21A/VD10x that have a DSA license installedARTG Number: 102177
  • Clasificación del producto
    Radiology Devices
  • Manufacturer
    Siemens Ltd

Manufacturer

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