Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1190-2025 — Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 12.0.0.932, 12.1.0.1221, 12.0.3.68, 12.0.4.12 and 12.3.0.119 Software Version: RayStation 11B and 11B Service Pack 1, 2, 3 and Service Pack Toshiba 1

U.S. FDA — Device Enforcement · Sweden · 2025-01-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1190-2025
Date of alert
2025-01-16
Country / jurisdiction
Sweden
Risk level
Class II
Risk type
recall
Brand
RAYSEARCH LABORATORIES AB
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
07350002010426
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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