Events

Field Safety Notices about iPlan RT Dose

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 Brainlab.

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
    2015-06-12
  • Event Country
    Slovenia
  • Event Source
    AMPMDRS
  • 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
    We are writing to advise you of the following effect that has been identified for the usage of iplan rt dose radiation treatment planning software version 4.0 or 4.1 (including all subversions: 4.0, 4.1.0, 4.1.1, 4.1.2, 4.1.3, 4.1.4). please note that version 4.1 is not the latest version of iplan rt. the purpose of this product notification letter is to provide you with corrective action information and to advise you of the actions brainlab is taking to address the issue. .

Device

iPlan RT Dose

Manufacturer

Brainlab