ClearanceBrief
Recall Z-1339-2022 ยท OWB Interventional Fluoroscopic X-Ray System

Siemens Medical Solutions USA, Inc

syngo Application software VE20 (Material Number 10848815) installed on the Artis pheno and Artis icono systems as follows: (1) Artis pheno Model Number:10849000 (2) Artis icono biplane Model Number: 11327600 (3) Artis icono floor Model Number: 11327700

DateFeb 25, 2022
StatusOpen, Classified
ReasonAfter CT image data from Toshiba is loaded, image mirroring can occur along the horizontal and vertical image axes. If this error occurs, the patient orientation/position may be misinterpreted and result in inappropriate treatment, even if the incorrect visualization is obvious.
Root causeSoftware design
ActionSiemens Medical Solutions USA, Inc. initiated a Customer Safety Advisory Notice to customers via AX007/22/S dated 2/25/22. Letter states reason for recall, health risk and action to take: We do not consider it necessary to re-examine any patients previously treated using the syngo application software. Siemens will correct the software error via Update Instruction AX006/22/S. Our service organization will contact you shortly to arrange a date to perform this corrective action. Please feel free to contact our service organization for an earlier appointment at 1-800-888-7436. Following th
Quantity127 units
DistributionUS Nationwide.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K163286ARTIS pheno
Siemens Medical Solution USA, Inc., Mar 9, 2017
K190768ARTIS icono
Siemens Medical Solutions USA, Inc., Sep 12, 2019
K193326ARTIS Icono
Siemens Medical Solutions USA, Inc., Apr 16, 2020
K201156ARTIS pheno (VE2)
Siemens Medical Solution USA, Inc., Jun 29, 2020