Recall of Brianlab iPlan RT Image (versions below v.4.1.2) / iPlan RT and BrainSCAN (discontinued in 2002) (Radiation therapy treatment planning system)

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Brainlab Australia 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-2015-RN-01021-1
  • Event Risk Class
    Class I
  • Event Initiated Date
    2015-10-20
  • 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
    The only image sets that are supported by the brainlab radiation treatment planning software even when containing varying calibrations of pixel values in between image slices are ct image sets & pet image sets normalised to suv with suv also loaded in and displayed by the brainlab swif such an unsupported image set is used the same pixel value calibration as contained in the middle image slice of the set to all slices is applied. in a pet image set uniform calibrated pixels might then have a different activity value, thus displayed with a different brightness and colour, compared to the image slices as displayed by the scanner using varying calibrations. if this effect occurs when using an unsupported image set, it can be misleading to the user during treatment planning and result in an incorrect definition of vols of interest in the planning s/w. the objects created for these vols of interest might differ in location or dimension from the actual desired definition of the structure.
  • Action
    Brainlab will provide a software solution with the corresponding new feature for affected iPlan RT / iPlan RT Image customers to prevent the described scenario from occurring. In the interim, customers are advised to: - Except for CT and PET used with SUV, only load and use image sets in iPlan RT / iPlan RT Imagethat have the same pixel value calibration for all images of the set. - Before using image datasets loaded into the Brainlab Radiation Treatment Planning Software, always compare the images displayed in the Brainlab application to the images as displayed by the imaging device (scanner). Delete and do not use the image sets within iPlan RT in case any deviation is detected and contact Brainlab support. Brainlab will not provide a software update for BrainSCAN. Brainlab strongly recommends customers still using BrainSCAN clinically to phase out the use of this software as soon as possible but in no event later than January 2016. This action has been closed-out on 02/12/2016.

Device

  • Model / Serial
    Brianlab iPlan RT Image (versions below v.4.1.2) / iPlan RT and BrainSCAN (discontinued in 2002) (Radiation therapy treatment planning system)ARTG Number: 121114
  • Manufacturer

Manufacturer