ClearanceBrief
Recall Z-2031-2019 ยท OWB Interventional Fluoroscopic X-Ray System

Siemens Medical Solutions USA, Inc

Artis zee biplane, Model Number 10094141

DateJun 12, 2019
StatusTerminated
ReasonA tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
Root causeComponent design/selection
ActionUrgent Medical Device Correction notification letters dated 6/12/19 were sent to customers. In the event the issue occurs, the system cannot be operated normally as X-ray will not possible. Planned procedures may have to be terminated and performed on an alternative X-ray system. Siemens advises that an alternative system is available to continue treatment in case of occurrence. Siemens is implementing a corrective action to all potentially affected users of the Artis Zee and AXIOM Artis systems with generator A100 via Update Instruction AX038/18/S. The Siemens Service organization will mo
Quantity268
DistributionUS Nationwide Distribution
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K181407Artis zee/zeego & Artis Q/Q.zen
Siemens Medical Solution USA, Inc., Aug 15, 2018