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FDAJune 1, 2022device

RayStation 9B SP1. For radiation treatment planning.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

An issue with propagation of treatment course information from RayStation with RayTreat to RayCare has been identified. During some workflows, information may not be propagated to RayCare.

What to do

FDA enforcement status: Terminated

Brands named

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Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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