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 zeego- Serial number

    140 of 140 codes

    • 160851
    • 160879
    • 160943
    • 160484
    • 160909
    • 160502
    • 160817
    • 160999
    • 160449
    • 160852
    • 160834
    • 160972
    • 160463
    • 160944
    • 160823
    • 160994
    • 160959
    • 160913
    • 160886
    • 160961
    • 160506
    • 160845
    • 160877
    • 160488
    • 160997
    • 160864
    • 160937
    • 160965
    • 160800
    • 160455
    • 160884
    • 160486
    • 160435
    • 160451
    • 160951
    • 160431
    • 160448
    • 160925
    • 160916
    • 160814
    • 160872
    • 160493
    • 160905
    • 160470
    • 160915
    • 160447
    • 160471
    • 160481
    • 160871
    • 160989
    • 160501
    • 160869
    • 160874
    • 160862
    • 160438
    • 160860
    • 160900
    • 160450
    • 160854
    • 160878
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.