Recall of syngo RT Oncologist with software version 4.2.X or 4.3.X (image processing device that can be a component of one or more radiation therapy systems)

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Siemens Healthcare Pty Ltd.

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
    RC-2016-RN-01087-1
  • Event Risk Class
    Class II
  • Event Initiated Date
    2016-08-18
  • Event Country
  • Event Source
    DHTGA
  • Event Source URL
  • Notes / Alerts
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 Australia.
  • Extra notes in the data
  • Reason
    Siemens are advising users regarding a bundled update of the syngo rt oncologist software. the update addresses the following issues:- incorrect offset calculation in adaptive targeting option. in rare cases, an identical region of interest (roi) label for the planning isocenter and the treatment isocenter may have been randomly generated during image processing. in this case the offset calculation in adaptive targeting during image review has been incorrect. - problems with structure name in case of using structure operation functionality in segmentation. in special scenarios within the structure operation functionality of the segmentation tab, the system did not store the selected name from the list of predefined names when creating a new structure. after reloading the data, the system replaced the name of this structure by the name of the former last deleted structure.There have been no reports of injuries as a result of the reported issues.
  • Action
    Siemens is advising users of the potential issues in order for users to maintain awareness until the software correction is implemented as a permanent correction. This action has been closed out on 16 June 2017.

Device

  • Model / Serial
    syngo RT Oncologist with software version 4.2.X or 4.3.X (image processing device that can be a component of one or more radiation therapy systems)ARTG Number: 181846
  • Manufacturer

Manufacturer

  • Manufacturer Parent Company (2017)
  • Source
    DHTGA