Recall of ARTISTE MV - LINEAR ACCELERATOR - SYNGO RT THERAPIST ASSIST

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by SIEMENS CANADA LIMITED - HEALTHCARE.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    101989
  • Event Risk Class
    III
  • Event Initiated Date
    2011-03-28
  • Event Country
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Extra notes in the data
  • Reason
    There is a potential safety risk related to patient treatment when using the portal review application of the syngo rt therapist. as a consequence of this risk an incorrect offset may be applied for patient positioning and thus may result in a mistreatment (dose to wrong location).

Device

  • Model / Serial
    Model Catalog: 08162807 (Lot serial: 10024); Model Catalog: 08162807 (Lot serial: 10048); Model Catalog: 08162815 (Lot serial: 10003); Model Catalog: 08162815 (Lot serial: 10040)
  • Product Description
    ARTISTE MV-LINEAR ACCELERATOR-SYNGO RT THERAPIST
  • Manufacturer

Manufacturer

  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
  • Source
    HC