Data Foundry

Medical device recalls 2020

RayStation stand-alone software treatment planning system — Class II medical device recall Z-0866-2020

Terminated recall by RAYSEARCH LABORATORIES AB, reported 2020-02-05, distributed nationwide. Three issues found: i) The Map ROI options in the ROI list in the Structure Definition module may generate uni

Recall numberZ-0866-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmRAYSEARCH LABORATORIES AB, Stockholm, N/A, Sweden
Recall initiated2019-12-19
Classified2020-02-04
Reported by FDA2020-02-05
Terminated2020-11-24
DistributedNationwide (US)
Quantity3,114 devices
Model numbers4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3, 7.0, 8.0, 8.1, 9.0

Product

RayStation stand-alone software treatment planning system. Models 4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3, 7.0, 8.0, 8.1, 9.0.

Reason for recall

Three issues found: i) The Map ROI options in the ROI list in the Structure Definition module may generate unintended ROI geometries ii) Elekta guard leaf behavior. There is an interoperability issue with Elekta regarding setting of guard leaves. iii)SSD, when intended as source-to-surface distance, it sometimes gives source-to-skin distance.To the best of our knowledge, these issues have not caused any patient mistreatment or other incidents. However, the user must be aware of the following information to avoid incorrect dose calculations during treatment planning.

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-0866-2020. 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.