Reported Mar 25, 2020 · Terminated

Artis zee Biplane, Model No. 10094141; Artis zee Ceiling, Model No. 10094137; Artis zee Floor, Model No. 10094135;…

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?

4 of 4 products

Products covered by this recall
Model / numberProduct as published
10094141Artis zee Biplane
10094137Artis zee Ceiling
10094135Artis zee Floor
10280959Artis zeego, Product Usage: Artis 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.
Lot codes and dates
  • Serial Numbers

    276 of 276 codes

    • 154827
    • 160851
    • 148262
    • 155168
    • 154408
    • 148299
    • 137623
    • 137714
    • 125213
    • 125238
    • 125245
    • 160869
    • 147573
    • 126202
    • 161046
    • 161041
    • 154454
    • 153834
    • 147581
    • 147857
    • 147562
    • 154532
    • 147983
    • 161218
    • 160999
    • 161032
    • 161204
    • 125001
    • 161226
    • 147604
    • 153890
    • 154721
    • 154722
    • 137193
    • 138055
    • 147760
    • 147923
    • 160449
    • 160834
    • 160852
    • 138035
    • 160944
    • 137479
    • 146245
    • 160994
    • 154567
    • 160959
    • 147803
    • 125249
    • 125241
    • 154704
    • 160913
    • 148260
    • 138087
    • 160886
    • 148335
    • 154086
    • 138112
    • 161206
    • 147841
    ***Added 11/2/20*** 153640 146855 160493 154572 160967 147813
Amount recalled
1452 worldwide (638 US)

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide

Why it was recalled

A software issue could potentially cause the stand and table movements to be blocked.

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 Apr 20, 2021 · Data as of Sep 19, 5:30 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.