Product Safety Recalls

Product Recall Tracker


Description: RayStation (Treatment Planning System) Model Number RayStation is , , , , , , , , , , , , , , or .

RAYSEARCH LABORATORIES AB Recall 87977 Information

Mandated?Voluntary: Firm initiated
Recall NumberZ-1838-2021
Event ID87977
Event DescriptionRayStation (Treatment Planning System) Model Number RayStation is , , , , , , , , , , , , , , or .
Product TypeDevices
DistributionWorldwide distribution - US Nationwide distribution in the states of AK, AL, AZ, CA, CT, DC, DE, FL, GA, HI, ID, IL, LA, MA, MD, ME, MI, MO, MS, MT, NC, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI and the countries of Algeria, Australia, Austria, Bahrain, Belgium, Canada, Colombia, Czech Republic, Denmark, Egypt, Estonia, France, French Polynesia, Germany, Hong Kong, China, India, Indonesia, Iran, Israel, Italy, Japan, Korea, Malaysia, Morocco, Netherlands, New Zealand, Norway, Poland, Qatar, Singapore, Slovenia, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, UAE, UK,
QuantityDomestic: 13,722 systems
Recall ReasonEvaluation of a clinical goal for the voxelwise worst dose distributions may be misleading after editing the clinical goal. It also describes an issue with contouring when the spacing between slices is d 1 mm, present in RayStation/RayPlan versions from 6 up to 10A.
Device Classification20210616
Device Code InfoSoftware version: RayStation 6, 7, 8A, 8B, 9A, 9B, 10A, 10B, RayPlan 2 including some service packs.
Center Classification Date20210609
Recall Initiation Date20210421
Initial Notification Letter
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied. is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.