Siemens Medical Solutions USA, Inc 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. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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.
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
Serial Number 133527
Products Sold
Serial Number 133527
Siemens Medical Solutions USA, Inc is recalling syngo.via RT Image Suite upgraded to VB60 running on syngo.via Model Number 10496180. Running on se due to Upgraded software version makes an automatic change in laser configuration settings for "markerless workflow" which may lead to the wrong laser offset. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
4/4/22 update: Urgent Medical Device Correction letter has not been issued. The proposed letter informs customers of software issue and workaround to resolve issue. It also requires electronic signature to acknowledge receipt of the notification. If you have additional questions contact the service organization at 1-800-888-7436.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026