Rappel de Siemens syngo.Plaza Imaging System

Selon New Zealand Medicines and Medical Devices Safety Authority, ce/cet/cette rappel concerne un dispositif en/au/aux/à New Zealand qui a été fabriqué par Siemens AG.

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    17987
  • Date de mise en oeuvre de l'événement
    2016-01-14
  • Pays de l'événement
  • Source de l'événement
    NZMMDSA
  • URL de la source de l'événement
  • Notes / Alertes
    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.
  • Notes supplémentaires dans les données
    Recalling Organisation: Siemens Healthcare (NZ) Ltd, Millennium Centre, Part Level 2, Building A, 600 Great South Road, Ellerslie, AUCKLAND 1051
  • Cause
    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.
  • Action
    Software to be upgraded

Device

  • Modèle / numéro de série
    Model: Catalogue Number: 10863171 & 10592457, Affected: , Software version: All versions
  • Manufacturer

Manufacturer

  • Société-mère du fabricant (2017)
  • Source
    NZMMDSA