---
title: "syngo.via RT Image Suite upgraded to VB60 running on syngo.via Model Number 1... — FDA record Z-0994-2022 | Is It on Recall"
description: "Upgraded software version makes an automatic change in laser configuration settings for \"markerless workflow\" which may lead to the wrong laser offset coordinat"
url: https://isitonrecall.com/recall/fda-device-z-0994-2022-syngo-via-rt-image-suite-upgraded-to-vb60-running-on-syngo-via-model-number-10496180-running-on-serv/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# syngo.via RT Image Suite upgraded to VB60 running on syngo.via Model Number 10496180. Running on servers with syngo.v... — FDA record Z-0994-2022

Reported terminated

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 Mar 7, 2022. 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**: syngo.via RT Image Suite upgraded to VB60 running on syngo.via Model Number 10496180. Running on servers with syngo.via VB60 software after upgrade and CT scanners with syngo.CT VA40A after upgrade.
- **Reason**: Upgraded software version makes an automatic change in laser configuration settings for "markerless workflow" which may lead to the wrong laser offset coordinates being displayed in the Patient Marking step.
- **Classification**: Class II
- **Recalling firm**: Siemens Medical Solutions USA, Inc
- **Quantity**: 1 (US)
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0994-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0994-2022%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 | Serial Number 133527 |

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

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, IL, IN, KY, MD, MO, ND, NH, NY, OH, OR, PA, SD, TX, VA and the countries of Argentina, Austria, Bahrain, Belgium, Brazil, Czechia, Denmark, France, Germany, Hungary, India, Italy, Japan, Netherlands, Norway, Poland, Romania, Slovakia, Spain, Switzerland, United Kingdom.

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**: May 4, 2022
- **Recall initiation date**: Mar 7, 2022
- **Center classification date**: Apr 22, 2022
- **Termination date**: Dec 19, 2023

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-0994-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Siemens Medical Solutions USA, Inc records](https://isitonrecall.com/brand/siemens-medical-solutions-usa-inc/)
