FDA Enforcement Class II Terminated

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 radiographic/fluoroscopic procedures as well as procedures next to the table for patient extremities.

Recall: Z-1282-2016 · Reported April 6, 2016

Enforcement

Recall Number
Z-1282-2016
Event ID
73606
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Siemens Medical Solutions USA, Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
April 6, 2016
Initiation Date
March 11, 2016
Classification Date
March 31, 2016
Termination Date
November 17, 2017
Address
40 Liberty Blvd, N/A, Malvern, PA, 19355-1418, United States

Description

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 radiographic/fluoroscopic procedures as well as procedures next to the table for patient extremities.

Reason

After 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.

Code Info

Serial # 82010, material # 10848600

Distribution

Nationwide Distribution to Michigan only

Quantity

1 angiography system