Recall Z-2686-2017

Siemens Medical Solutions USA, Inc · initiated February 3, 2017

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Artis zee,x-ray system, angiographic Artis zee is 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 include cardiac angiography, neuro angiography, general angiography, rotational angiography, operating room angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures. Artis zee systems can also support the acquisition of position triggered imaging for spatial data synthesis

Codes / lots: Serial Numbers: 124081 124061 137662 137668 137391 148001 147871 154827 154847 153197 131101 154035

Reason for recall

Failures can result due to a component defect on Artis zee systems with an A100 Plus generator of a certain delivery lot and 2-focus Megalix Cat Plus tube unit.

FDA-determined cause: Component design/selection

Action taken

CDRH approved the CAP subject to the following conditions: 1. You completed this recall as of May 6, 2017. Report any failures regarding this recall immediately to the District Recall Coordinator. 2. If this recall is expanded to include any additional consignees, models, or end users, any future customer notification letters to be sent must comply with the requirements of 21 CFR 1003.21. This includes, but is not limited to, the prescribed packaging and the statement that you will remedy the defect or bring the product into compliance at no charge.

Details

Recall number
Z-2686-2017
Initiated
February 3, 2017
Terminated
October 24, 2017
Product code
IZI – System, X-Ray, Angiographic
Quantity
97 distributed worldwide, 12 distributed in United States
Distribution
Worldwide Distribution - US to AR, KS, MI, IA, IL, WI, MN, WV, OH, and NY
Recalling firm
Siemens Medical Solutions USA, Inc, Malvern, PA

Official FDA recall record