ClearanceBrief
Recall Z-0601-2017 ยท OWB Interventional Fluoroscopic X-Ray System

Siemens Medical Solutions USA, Inc

Artis Q, Angiographic x-ray system Product Usage: The Artis systems are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed with the Artis zee / zeego and Q/ Q.zen include cardiac angiography, neuro angiography, general angiography,

DateNov 17, 2016 (initiated Nov 1, 2016)
StatusTerminated
ReasonThe possibility exists that the semi-automatic focus switch may not work as intended when pressing the footswitch multiple times.
Root causeSoftware in the Use Environment
ActionSiemens mailed a Customer Safety Advisory Notice to affected customers to inform them of a corrective action they plan to perform to prevent a possible hazard to persons and equipment. The notice identified the associated risks, underlying issues, impact on system operation and actions to be taken.
Quantity4,657 systems (worldwide)
DistributionUS Nationwide Distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K123529ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM
Siemens Medical Solutions USA, Inc., Feb 26, 2013