RayStation 9B SP1. For radiation treatment planning recall
RayStation 9B SP1. For radiation treatment planning.
Why was RayStation 9B SP1. For radiation treatment planning recalled?
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 should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI: 0735000201029720200310 Build number 9.2.0.483
- Product
- RayStation 9B SP1. For radiation treatment planning.
- Recalling firm
- RAYSEARCH LABORATORIES AB
- Quantity
- 1
- Distribution
- Worldwide distribution - US Nationwide distribution in the state of TN and the countries of Belgium and Switzerland.
- Recall date
- July 27, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)