Reported Dec 1, 2021 · Terminated

Artis Q ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and…

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 Q ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and
  • interventional procedure Model Number10848281
Lot codes and dates
  • Serial Numbers

    67 of 67 codes

    • 110088
    • 110059
    • 110103
    • 110035
    • 110046
    • 110005
    • 110058
    • 110056
    • 110062
    • 109523
    • 109645
    • 110067
    • 110095
    • 110051
    • 110001
    • 110020
    • 110007
    • 110093
    • 110069
    • 110075
    • 109627
    • 110042
    • 110043
    • 110048
    • 110061
    • 110063
    • 110064
    • 110032
    • 110047
    • 110102
    • 110039
    • 110040
    • 110023
    • 110065
    • 110052
    • 110018
    • 110072
    • 110081
    • 110036
    • 110054
    • 110053
    • 110044
    • 110031
    • 110016
    • 110037
    • 110077
    • 109497
    • 110079
    • 110099
    • 110027
    • 110049
    • 110066
    • 110024
    • 110017
    • 110025
    • 110100
    • 110083
    • 110091
    • 110006
    • 110055
  • Expanded Recall 11/15/21110096 110014
Amount recalled
67 units

This recall covers 17 products

The agency filed one notice per product. You are reading one of them; the other 16 are below.

4 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

If SID (source-to-image distance) lift movement is activated and x-ray shall be released simultaneously; x-ray is not possible and the message No x-ray, try again is displayed, may result in a short delay in procedure

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 Jun 18, 2024 · Data as of Sep 19, 5:37 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.