Retiro De Equipo (Recall) de Siemens syngo.Plaza Imaging System

Según New Zealand Medicines and Medical Devices Safety Authority, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en New Zealand que fue producido por Siemens AG.

¿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
    17987
  • Fecha de inicio del evento
    2016-01-14
  • País del evento
  • Fuente del evento
    NZMMDSA
  • URL de la fuente del evento
  • Notas / Alertas
    Data from New Zealand is current through July 2018. All of the data comes from the New Zealand Medicines and Medical Devices Safety Authority, 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 New Zealand.
  • Notas adicionales en la data
    Recalling Organisation: Siemens Healthcare (NZ) Ltd, Millennium Centre, Part Level 2, Building A, 600 Great South Road, Ellerslie, AUCKLAND 1051
  • Causa
    In case of a system crash images may not be written to the hard disk and there may be inconsistencies in the database. when a system crash occurs (e.G. blue screen, power outage), images may not be written from cache to the hard disk and are lost. in such a case an existing file name identifier might be re-used after restart of the system. now two references to the same image file on sts exist in the database of syngo.Plaza., manufacturer has now released another version of the software as a final correction to this this action (sy099/14/s) . this software update will fix any inconsistencies in the archived data that may have occurred before software update vb10a_hf06 was installed.
  • Acción
    Software to be upgraded

Device

  • Modelo / Serial
    Model: Catalogue Number: 10863171 & 10592457, Affected: , Software version: All versions
  • Manufacturer

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Source
    NZMMDSA