device · product 1 of 1
Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283), Interventional Fluoroscopic X-Ray System
- Recall number
- Z-1343-2022
- Initiated
- May 24, 2022
- Classification
- Class II
- Status
- Terminated
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 233 worldwide; 32 US
App-derived interpretation
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.
Official device-enrichment evidence · Sourced
Component design/selection
Inspect official wording and provenance
Reason for recall
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.
Code information
UDI-DI: Artis zeego 04056869010083 Artis Q.zeego 04056869010007
Distribution pattern
Worldwide 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.