Alerte De Sécurité sur FastPlan treatment planning system

Selon Department of Health, ce/cet/cette alerte de sécurité concerne un dispositif en/au/aux/à Hong Kong qui a été fabriqué par Varian Medical Systems.

Qu'est-ce que c'est?

Les alertes fournissent des informations importantes et des recommandations concernant les dispositifs médicaux. Le fait qu'une alerte soit émise ne signifie pas nécessairement qu'un dispositif soit dangereux. Les alertes de sécurité, qui sont envoyées tant aux travailleurs du secteur médical qu'aux utilisateurs de ces dispositifs, peuvent inclure des rappels. Elles peuvent être rédigées par des fabricants mais aussi par des autorités en charge de la santé.

En savoir plus sur les données ici
  • Type d'événement
    Safety alert
  • Date
    2012-03-20
  • Pays de l'événement
  • Source de l'événement
    DH
  • URL de la source de l'événement
  • Notes / Alertes
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
  • Notes supplémentaires dans les données
    Medical Device Safety Alert
  • Cause
    Field safety notice: varian fastplan treatment planning system medical device manufacturer, varian medical systems (varian), has issued a field safety notice concerning fastplan treatment planning system. according to varian, an anomaly has been identified with the ct localization module of the fastplan treatment planning system. if the module reports a significant difference in tilt or spin on a slice (compared to the average of all slices) and the user elects to “discard” that slice, an incorrect calculation of the isocenter location may result. if this issue goes undetected, the reported coordinates of the isocenter will be incorrect and a mistreatment could result. varian is notifying all possibly affected customers with a field safety notice. according to varian, the affected devices were distributed to hong kong. if you are in possession of the products, please contact your supplier for necessary actions.

Device

  • Modèle / numéro de série
  • Description du dispositif
    Medical Device Safety Alert: Varian Eclipse™ Treatment Planning System
  • Manufacturer

Manufacturer