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Recall Observatory FDA recall evidence

Device product

Artis zee/zeego, Angiographic x-ray system Stand alone system 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, rotational angiography, operating room angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures. Artis zee/ zeego and Q/ Q.zen can also support the acquisition of position triggered imaging for spatial data synthesis.

Z-0971-2017

December 08, 2016

Class II

Product summary

Firm
Siemens Medical Solutions USA, Inc
Event
Event 76016
Status
Terminated
Classification
Class II
Quantity
1,500 distributed Worldwide
Official record key
device-enforcement:Z-0971-2017

Official wording

Reason: Siemens initiated a corrective action to address two possible, mutually independent causes of a system defect related to the following: - In Artis Systems with A100 Plus or A100G generators, an attempt to resume operation following detection of a fault can result in the failure of a module in the high-voltage generator. - For biplane systems delivered with software version VD11B since April of this year, software problems in conjunction with graphics card may, in rare cases, result in the loss of image display in the examination room.

Code information: Model # 10094135, 10094137, 10094139, 10094141, 10280959, 10848283

Distribution pattern: Nationwide Distribution

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software version VD11B since April of this year, software problems in conjunction with graphics card may, in rare cases, result in