Field Safety Notices about Artis one systems

According to Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), this field safety notices involved a device in Slovenia that was produced by Siemens Shenzhen Magnetic Resonance Ltd.

What is this?

Field safety notices are communications sent out by medical device manufacturers or their representatives in relation to actions that they may be taking in relation to their product that is on the market. These are mainly for health workers, but also for users. They can include recalls and alerts.

Learn more about the data here
  • Type of Event
    Field Safety Notice
  • Date
  • Event Country
  • Event Source
  • Notes / Alerts
    Data from Slovenia is current through February 2019. All of the data comes from the Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), 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 Slovenia.
  • Extra notes in the data
  • Reason
    During regular field observation, er (examination room) monitor display was identified with blinking, blue/black screen issues. what is the impact on system operation and what is the potential risk? in case the problem occurs, the impact to an ongoing procedure may be limited functionality up to failing of a system. in most of cases, a power circle (shutdown and then power on) can bring system back to normal. in very rare case while power circle does not work, it might be necessary to cancel or restart a clinical procedure or transferring it to a functioning system.



  • Manufacturer Parent Company (2017)
  • Source