ClearanceBrief
Recall Z-1282-2016 ยท OWB Interventional Fluoroscopic X-Ray System

Siemens Medical Solutions USA, Inc

Artis One, Interventional, Fluoroscopic, x-ray system Artis one is an angiography system developed for diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed with the Artis One include cardiac angiography, neuro-angiography, general angiography, rotational angiography, multipurpose angiography and whole body ra

DateMar 11, 2016
StatusTerminated
ReasonAfter importing segmentation results of the left atrium created on the Artis One system, the possibility exists for the results to be mirrored to an electro-anatomical 3D mapping system, CARTO from Biosense Webster Inc.
Root causeSoftware in the Use Environment
ActionSiemens mailed an Important Customer Safety Notice to customers to inform them of the issue and the corrective actions they plan to take to address the problem. The letter stated that Siemens service organization will contact customers to arrange a date for the installation of the software update. Customers were instructed to call Siemens service organization for an appointment at 1-800-888-7436.
Quantity1 angiography system
DistributionNationwide Distribution to Michigan only
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K133580ARTIS ONE
Siemens Medical Solutions USA, Inc., Apr 28, 2014