Product Safety Recalls

Product Recall Tracker

Siemens Medical Solutions USA, Inc Recall 90407

Description: Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283), Interventional Fluoroscopic X-Ray System

Siemens Medical Solutions USA, Inc Recall 90407 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-1343-2022
Event ID90407
Event DescriptionArtis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283), Interventional Fluoroscopic X-Ray System
Product TypeDevices
DistributionWorldwide distribution - US Nationwide distribution in the states of AL, AR, CA, CO, FL, IL, LA, ME, MN, MO, NC, OH, PA, SC, TN, TX, WI and the countries of Australia, Austria, Azerbaijan, Belgium, Canada, China, Finland, France, Germany, Hong Kong, India, Italy, Japan, Lebanon, Lithuania, Luxembourg, Netherlands, Poland, Portugal, South Korea, Switzerland, United Kingdom.
Quantity233 worldwide; 32 US
Recall ReasonIt may occur that after system startup no stand movement is possible any longer in the event of a discharged BIOS battery of the robotic stand control PC. If this problem occurs during startup, all stand movements are blocked and can only be reactivated by a field service engineer.
Device Classification20220713
Device Code InfoUDI-DI: Artis zeego 04056869010083 Artis Q.zeego 04056869010007
Center Classification Date20220707
Recall Initiation Date20220524
Recalling FirmSiemens Medical Solutions USA, Inc
Initial Notification Letter
Similar To

© 2021 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.