RegWardenFDA facility compliance records
Recall

Class II — RAYSEARCH LABORATORIES AB

Recalling firmRaySearch Laboratories AB (publ)
Registered facilityView this company's 2 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass II
StatusTerminated
ReasonWhen calculating electron Monte Carlo dose with a very large number of histories, the dose calculation may be wrong
ProductRayStation 3.5, RayStation 4.0, RayStation 4.5, RayStation 4.7, RayStation 5, RayStation 6, RayPlan 1 (RayStation 4.9) and RayPlan 2 (RayStation 6) . Intended Use: software system designed for treatment planning and analysis of radiation therapy
Quantity744
DistributionUS Nationwide Distribution
Initiated2017-11-20
Classified2019-07-03
Terminated2023-08-08
Recall numberZ-1930-2019
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — RAYSEARCH LABORATORIES AB (Z-1930-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83152/

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