Device recalls

Brand Name: RayStation Intended as a Radiation Therapy Treatment Planning System. Model/Catalog Number: 7.0.0.19, 8.0.0.61, 8.0.1.10 Softwa…

RAYSEARCH LABORATORIES AB · Inconsistency in the use of Density uncertainty in the RayStation functions Robust optimization, Robust evaluation and Compute perturbed dose for proton and li…

Open, ClassifiedUnder Investigation by firmZ-1185-2025
Open FDA's page for this record
Cfres ID
212150
Product res number
Z-1185-2025
Event date initiated
2025-01-16
Event date posted
2025-02-19
Recall status
Open, Classified
Res event number
96156
Product code
MUJ
Firm FEI number
3007774465
Recalling firm
RAYSEARCH LABORATORIES AB
Address 1
Eugeniavagen 18c 18c eugeniavagen
City
Stockholm
Country
Sweden
Additional info contact
Olympiada Lachana +46-85-1053000
Root cause description
Under Investigation by firm
Product quantity
0
Product description

Brand Name: RayStation Intended as a Radiation Therapy Treatment Planning System. Model/Catalog Number: 7.0.0.19, 8.0.0.61, 8.0.1.10 Software Version: RayStation 7, 8A and 8A Service Pack 1

Code info

Lot Code: UDI: 0735000201006820171130, 0735000201011220180608 and 0735000201013620180928 GTIN: 07350002010068, 07350002010112 and 07350002010136 Serial Numbers: 7.0.0.19, 8.0.0.61 and 8.0.1.10 Software Revision: RayStation 7, 8A and 8A Service Pack 1 Expiration Date: 2023-10-04

Reason for recall

Inconsistency in the use of Density uncertainty in the RayStation functions Robust optimization, Robust evaluation and Compute perturbed dose for proton and light ion treatment plans when a HU-to-mass density CT calibration curve used in RayStation version 4.5 to 2024B including some service packs.

Action

Raysearch issued Field Safety Notice, Medical Device Correction #148655 RayStation version 4.5 to 2024B including some service packs via email on 1/17/25. Letter states reason for recall, health risk and action to take: For users of HU-to-mass density CT calibration curves If a user wants to evaluate a plan with respect to relative stopping power/WE range error rather than mass density errors, there are two options: Option 1. Use a HU-to-SPR CT calibration curve instead of a HU-to-mass density curve. " For evaluation of an existing case, the evaluation can be done on an anonymized and exported copy of the patient and plan. " Contact RaySearch Service if you need help with the creation of a HU-to-SPR curve from an existing HU-to-mass density curve. Option 2. Evaluate the plan using a higher (effective) mass density uncertainty that gives similar relative stopping power and WE range change as the nominal value. " The following values of Effective mass density errors that give similar result as an intended Stopping power error have been deduced from a limited set of patients: " For other values of intended Stopping power error, interpolate the approximate Effective mass density value from the table above. " The values are estimates based on a few patients and are expected to vary slightly depending on the mass densities along the beam path. " Note that the values are not symmetrical around 0. For users of HU-to-SPR CT calibration curves Be aware that the density uncertainty given in Robust evaluation, Compute perturbed dose and Robust optimization is used directly to scale stopping power and therefore WE range. Starting from RayStation v2025, scheduled for market release in April 2025 (subject to market clearance in some markets), the impact of the mass density uncertainty in Robust evaluation and Compute perturbed dose when using a HU-to-mass density CT calibration curve will be changed to harmonize with the other use cases. This means that as of RayStat

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Belgium ENG, Canada, China, China APactron, Denmark, France, Germany, Hong Kong S.A.R. China, India, Italy, Japan, Korea, Netherlands, Norway, Poland, Singapore, Spain, SwitzerlandENG, Taiwan, Thailand, UK.

K numbers
K180379
Harmonized identifiers (openFDA)
Device name
System, Planning, Radiation Therapy Treatment
Medical specialty description
Radiology
Regulation number
892.5050
Device class
2
K number
K092132, K090972, K992434, K020971, K993923, K002132, K013644, K234068, K993895, K062967, K151435, K252304, K131891, K062514, K031349, K974770, K181145, K242463, K152488, K250064, K140187, K991815, K101220, K081281, K161136, K032345, K141860, K101119, K260308, K112446, K053584, K180308, K193640, K242822, K243057, K133247, K032209, K102216, K183037, K071873 +218 more
Registration number
3015777306, 3010123525, 3009090417, 3019834893, 3019543601, 3014425747, 3004580128, 3003586672, 2434141, 1038814, 3022719374, 9617978, 3003873069, 3009302839, 3030564015, 3007791541, 3014873236, 3003768277, 1651102, 3003418325, 2939248, 3006579682, 2916710, 3000126629, 3004561814, 3016602874, 3025765259, 3033527281, 3002808157, 3016686005, 9611894, 3023344262, 8043933, 3022745617, 3007037519, 3013410552, 3004363352, 3003793371, 2030598, 3012039133 +16 more
FEI number
3015777306, 3010123525, 3009090417, 3019834893, 3019543601, 3002807880, 3014425747, 3003586672, 3004580128, 3002802883, 2434141, 3022719374, 1038814, 3003873069, 3009302839, 3030564015, 3007791541, 3014873236, 3008581796, 3003418325, 2939248, 3006579682, 2916710, 3000126629, 3004561814, 3016602874, 3025765259, 3002807741, 3033527281, 3002808157, 3016686005, 3023344262, 3022745617, 3007037519, 3013410552, 3004363352, 3003793371, 3012039133, 3015232217, 1000518731 +16 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.