RAYSEARCH LABORATORIES AB: Device Recall

Recall #Z-1195-2025 · 01/16/2025

Class II: Risk

Recall Details

Recall Number
Z-1195-2025
Classification
Class II
Product Type
Device
Recalling Firm
RAYSEARCH LABORATORIES AB
Status
Ongoing
Date Initiated
01/16/2025
Location
Stockholm, N/A, Sweden
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
0

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.

Product Description

Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 4.5.1.14, 4.7.2.5, 4.7.3.13, 4.7.4.4, 4.7.5.4 and 4.7.6.7 Software Version: RayStation 4.5.1, 4.7.2, 4.7.3, 4.7.4, 4.7.5 and 4.7.6

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.

Other Recalls by RAYSEARCH LABORATORIES AB

View all recalls by RAYSEARCH LABORATORIES AB →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.