The Recall Desk
HighFDA (Devices)·Z-2345-2020·Announced 2020-06-17

RayStation 8A Software Recall for Dose Calculation Error

RaySearch Laboratories is recalling RayStation 8A Service Pack 1 software due to a dose calculation error that could underestimate radiation therapy doses.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a medical device software error that could lead to incorrect radiation dosing, representing a risk of harm where injury has not yet been reported, consistent with the 'High' severity criteria.

Plain-English summary

RaySearch Laboratories AB is recalling RayStation 8A Service Pack 1, UDI # 07350002010136, Build number 8.0.1.10. This software is used for radiation therapy and medical oncology to administer treatments.

The recall was initiated because a software error was identified in the Pencil Beam Scanning (PBS) and Line Scanning (LS) dose calculation algorithms. This error could result in a local underestimation of the expected dose.

The product was distributed nationwide in the United States, including in Florida, Georgia, Utah, Virginia, California, Maryland, Arizona, Texas, Washington DC, Missouri, Massachusetts, Illinois, Oklahoma, New Jersey, Tennessee, and Louisiana. Users of this software should contact RaySearch Laboratories for further instructions.

The recalled product

Product
RayStation 8A Service Pack 1, UDI # 07350002010136 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • UDI # 07350002010136 Build number: 8.0.1.10

Distribution

Distributed nationwide across the United States.

The notice also names 17 states specifically:

Part of a larger recall action

This product is one of 15 recalled by RAYSEARCH LABORATORIES AB under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 15 products in this recall →