ClearanceBrief
Recall Z-0994-2022 ยท MUJ System, Planning, Radiation Therapy Treatment

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.

DateMar 7, 2022
StatusTerminated
ReasonUpgraded 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.
Root causeSoftware change control
Action4/4/22 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.
Quantity1 (US)
DistributionWorldwide 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,
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K211379syngo.via RT Image Suite
Siemens Medical Solutions USA, Inc., Jul 30, 2021