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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K240398
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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RayStation with the following product descriptions: 1. RayStation 2023B, Software Version: 14.0.... 2 09/02/2025 RAYSEARCH LABORATORIES AB
Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 14.0.0, 15.0.0, 15.1... 2 01/16/2026 RAYSEARCH LABORATORIES AB
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