Siemens Medical Solutions USA, Inc Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283), Interventional Fluoroscopic X-Ray System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283), Interventional Fluoroscopic X-Ray System
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
UDI-DI: Artis zeego 04056869010083 Artis Q.zeego 04056869010007
Products Sold
UDI-DI: Artis zeego 04056869010083 Artis Q.zeego 04056869010007
Siemens Medical Solutions USA, Inc is recalling Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283), Interventional Fluoroscopi due to It 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. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
It 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.
Recommended Action
Per FDA guidance
On May 24, 2022, the firm mailed Urgent Medical Device Correction letters to affected consignees. Customers were informed that if the system is not used regularly, please ensure that the system is switched on in due time before any use to check the status. Please ensure that patient treatment can be continued in other ways if there is any possible danger for the safety of the patient. The firm will replace the Bios battery and the service interval will be shortened to two years. The firm will contact customers to arrange a date to perform the correction. Customers may call the service organization at 1-800-888-7435 to schedule an earlier appointment.
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