---
title: "Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning Sy... — FDA record Z-1188-2025 | Is It on Recall"
description: "Inconsistency in the use of Density uncertainty in the RayStation functions Robust optimization, Robust evaluation and Compute perturbed dose for proton and lig"
url: https://isitonrecall.com/recall/fda-device-z-1188-2025-brand-name-raystation-intended-as-a-radiation-therapy-treatment-planning-system-model-catalog-number/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 10.1.0.613 an... — FDA record Z-1188-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jan 16, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 10.1.0.613 and 10.1.1.54 Software Version: RayStation 10B and 10B Service Pack 1
- **Reason**: Inconsistency in the use of Density uncertainty in the RayStation functions Robust optimization, Robust evaluation and Compute perturbed dose for proton and light ion treatment plans when a HU-to-mass density CT calibration curve used in RayStation version 4.5 to 2024B including some service packs.
- **Classification**: Class II
- **Recalling firm**: RAYSEARCH LABORATORIES AB
- **Quantity**: 0
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1188-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1188-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot Code: UDI: 0735000201031020201216 and 0735000201047120220128 GTIN: 07350002010310 and 07350002010471 Serial Numbers: 10.1.0.613 and 10.1.1.54 Software Revisions: RayStation 10B and 10B Service Pack 1 Expiration Date: 2027-02-01 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Belgium ENG, Canada, China, China APactron, Denmark, France, Germany, Hong Kong S.A.R. China, India, Italy, Japan, Korea, Netherlands, Norway, Poland, Singapore, Spain, SwitzerlandENG, Taiwan, Thailand, UK.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Feb 26, 2025
- **Recall initiation date**: Jan 16, 2025
- **Center classification date**: Feb 19, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1188-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [RAYSEARCH LABORATORIES AB records](https://isitonrecall.com/brand/raysearch-laboratories-ab/)
