Data Foundry

Medical device recalls 2012

Brand name: RayStation — Class II medical device recall Z-2324-2012

Terminated recall by RAYSEARCH LABORATORIES AB, reported 2012-09-12, distributed nationwide. The firm decided to recall when an issue was found with the dose calculation in RayStation 2.5, Raystation 2.5

Recall numberZ-2324-2012
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmRAYSEARCH LABORATORIES AB, Stockholm, N/A, Sweden
Recall initiated2012-05-09
Classified2012-09-06
Reported by FDA2012-09-12
Terminated2013-01-25
DistributedNationwide (US)
Countries outside the USCA, CH, DE, NL
Quantity19 units

Product

Brand name: RayStation. Generic name: Treatment Planning System. Software version and build numbers are 2.5.0.144 and 2.5.1.89. Product lifetime is 5 years. RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of dose distributions expected during the proposed treatment, and may be used to administer treatments after review and approval by the intended user. The system functionality can be configured based on user needs. The intended users of RayStation shall be clinically qualified radiation therapy staff trained in using the system.

Reason for recall

The firm decided to recall when an issue was found with the dose calculation in RayStation 2.5, Raystation 2.5.1. The problem has not caused any patient mistreatment or other incidents. However, the user must be aware of this information to avoid incorrect dose calculations during treatment planning. The dose calculation is not correctly normalized in the unusual case of preventing the optimizatio

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2324-2012. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.