RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden RayStation standalone software treatment planning system (RayStation 8A, 8B, 9A, and 9B, including all service packs) model no. 8.0, 8.1, 9.0, 9.1, 9.2 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
RayStation standalone software treatment planning system (RayStation 8A, 8B, 9A, and 9B, including all service packs) model no. 8.0, 8.1, 9.0, 9.1, 9.2
Brand
RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden
Lot Codes / Batch Numbers
Software versions 8.0.0.61, 8.0.1.10, 8.1.0.47, 8.1.1.8, 8.1.2.5, 9.0.0.113, 9.1.0.933 and 9.2.0.483
Products Sold
Software versions 8.0.0.61 , 8.0.1.10 , 8.1.0.47 , 8.1.1.8 , 8.1.2.5 , 9.0.0.113 , 9.1.0.933 and 9.2.0.483
RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden is recalling RayStation standalone software treatment planning system (RayStation 8A, 8B, 9A, and 9B, including a due to It is not obvious that the manual import of a treatment record into RayCare PACS does not automatically import the same data into RayTreat. In additio. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
It is not obvious that the manual import of a treatment record into RayCare PACS does not automatically import the same data into RayTreat. In addition, there is an issue found with the display of planned and recorded Gantry Angle in the delivered beam list in RayTreat.
Recommended Action
Per FDA guidance
On May 26, 2020, the firm notified affected customers of the product issue via emailed Field Safety Notices. Customers were made aware of the following issues: 1) When only a single beam record is received for a specific beam, the delivered Gantry angle is hidden and only the planned Gantry angle is shown, and 2) For users of RayCare 3B and RayStation RayTreat 9B (including all service packs), if a manual import is necessary, the treatment record must be imported manually into both RayStation and PACS. ACTIONS TO BE TAKEN BY THE USER " Be aware that the Gantry angle column in the first row for each beam in the Beam delivery results always shows the planned Gantry angle and does not indicate which Gantry angle was used when delivering a beam. " If treatment records are not successfully sent from the delivery machine to RayTreat: o always manually record all the beams that were delivered before signing off the session. o import all treatment records into both RayStation and RayPACS. " Take extra precautions when delivering a continuation session based on a manually recorded or offline imported treatment records to ensure that the correct amount of radiation is delivered during the continuation. " Educate treatment staff and all users about this workaround. " Inspect your product and identify all installed units with the above software version number(s). " Confirm you have read and understood this notice by replying to the notification email. The firm plans to resolve these issues in the next version of RayStation, which the firm estimates will be available in June 2020. If customers wish to continue using versions of RayStation affected by this notice, all users must maintain awareness of this notice. Alternatively, customers can choose to upgrade to the new version once it becomes available for clinical use.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IN
Page updated: Jan 10, 2026