Reported Mar 25, 2020 · Terminated

Artis Q Biplane, Model No. 10848282; Artis Q Ceiling, Model No.10848281; Artis Q Floor, Model No. 10848280; Artis Q…

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
10848282Artis Q Biplane
10848281Artis Q Ceiling
10848280Artis Q Floor
10848283Artis Q 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

    293 of 293 codes

    • 117316
    • 109490
    • 117021
    • 121396
    • 121185
    • 121430
    • 117012
    • 121406
    • 109141
    • 109502
    • 109123
    • 121336
    • 109400
    • 109210
    • 121089
    • 109080
    • 103061
    • 109190
    • 109191
    • 109197
    • 109198
    • 121013
    • 117136
    • 117324
    • 109418
    • 109419
    • 109421
    • 121040
    • 109405
    • 109437
    • 109119
    • 109346
    • 121445
    • 121082
    • 109460
    • 121459
    • 121011
    • 109137
    • 109512
    • 117108
    • 109300
    • 121371
    • 109187
    • 121134
    • 121374
    • 109228
    • 109412
    • 109066
    • 109067
    • 109068
    • 121053
    • 121054
    • 121422
    • 117001
    • 117023
    • 109133
    • 109134
    • 121014
    • 121112
    • 121209
    ***Added 3/30/20*** 109016 121062 109118 117034 117026 121190 109302
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, 4:53 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.