Reported Sep 6, 2017 · Terminated

Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated…

Siemens Medical Solutions USA, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Siemens Medical Solutions USA, Inc · 40 Liberty Blvd · Malvern, PA · 19355-1418

Is this the product you have?

  • Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen 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 AXIOM Artis-zee/zeego and Q/Q.zen family include cardiac angiography, neuro angiography, general angiography, rotational angiography, operating room angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures. AXIOM Artis zee/zeego and Q/Q.zen can also support the acquisition of position triggered imaging for spatial data synthesis
Lot codes and dates
  • Artis zee biplane- Serial number

    126 of 126 codes

    • 154502
    • 154616
    • 154536
    • 154096
    • 154454
    • 154715
    • 154789
    • 154779
    • 154532
    • 131017
    • 154157
    • 154722
    • 154721
    • 154571
    • 154074
    • 154612
    • 154090
    • 154658
    • 154686
    • 154095
    • 154567
    • 154480
    • 154093
    • 154086
    • 154704
    • 153882
    • 154727
    • 154408
    • 154509
    • 154079
    • 154462
    • 154098
    • 154073
    • 154076
    • 154792
    • 154156
    • 154799
    • 154814
    • 154783
    • 154731
    • 154683
    • 153878
    • 154565
    • 154653
    • 154671
    • 154556
    • 154406
    • 154518
    • 154778
    • 154685
    • 137650
    • 131005
    • 154633
    • 154020
    • 154058
    • 154155
    • 153884
    • 154453
    • 154708
    • 154579
Amount recalled
986 units in USA

This recall covers 12 products

The agency filed one notice per product. You are reading one of them; the other 11 are below.

Where it was sold

  • Nationwide

Why it was recalled

Due to a leak in the cooling system, fluids could potentially seep into the equipment cabinet. Loss of coolant can results in a cooling system failure and subsequent system failure. This leek can occur sporadically in affected systems.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 17, 2017 · Data as of Sep 19, 6:06 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.