Recall StatusTerminated
Date Initiated2019-11-18
Date Terminated2020-11-10
Product Quantity956 Devices/Licences
Reason for Recall
Editing a static arc beam may unexpectedly set the MU of the beam to its initial default value of 200 MU. If the bug is triggered, the dose is invalidated and needs to be recalculated before the plan can be approved or exported.
Firm Action
Field Safety Notice, Medical Device Correction notification letters dated 11/18/19 were sent to customers.
ACTIONS TO BE TAKEN BY THE USER
" Be aware that the MU of static arc beams may change unexpectedly when using the Edit beam dialog or when editing the beam aperture.
" Always review the final dose before approving a plan for treatment:
WARNING!
Plan review and approval. All treatment plan data shall be carefully reviewed and
approved by a qualified person before it is used for radiotherapy treatment purposes.
A plan (beam set) that is 'optimal' with respect to the optimization goals may still be inappropriate for clinical use. (508826, 508814)
Please educate planning staff and all users about this workaround.
Inspect your product and identify all installed units with the above software version number(s), then confirm that you have read and understood this notice by replying to the notification email.
SOLUTION
This issue will be resolved in the next version of RayStation/RayPlan, scheduled for market release in December 2019 (subject to market clearance in some markets). If customers wish to continue using versions of RayStation/RayPlan 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.
TRANSMISSION OF THIS NOTICE
This notice needs to be passed on to all those who need to be aware within your organization. Please maintain awareness of this notice as long as any version of RayStation/RayPlan affected by this issue is in use to ensure effectiveness of the workaround.
Root Cause
Software design
Distribution Pattern
US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, ID, IL, LA, MA, MD, ME, MI, MO, MS, MT, NC, NJ, NY, OH, OK, OR, PA, RI, TN, TX, UT, VA, VT, WA, and WI.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.