Reported Jul 10, 2019 · Terminated

Siemens Artis Q ceiling--Interventional Fluoroscopic X-Ray System Model Number: 10848281

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?

  • Siemens Artis Q ceiling--Interventional
  • Fluoroscopic X-Ray System Model Number10848281
Lot codes and dates
  • Serial Numbers

    131 of 131 codes

    • 109007
    • 109057
    • 109028
    • 109027
    • 109011
    • 109021
    • 109009
    • 109010
    • 109072
    • 109075
    • 109071
    • 109041
    • 109039
    • 109032
    • 109020
    • 109036
    • 109048
    • 109088
    • 109101
    • 109040
    • 109034
    • 109031
    • 109043
    • 109067
    • 109068
    • 109093
    • 109080
    • 109179
    • 109134
    • 109133
    • 109496
    • 109076
    • 109105
    • 109104
    • 109107
    • 109084
    • 109060
    • 109164
    • 109167
    • 109135
    • 109119
    • 109090
    • 109096
    • 109091
    • 109146
    • 109102
    • 109092
    • 109189
    • 109129
    • 109143
    • 109183
    • 109606
    • 109144
    • 109171
    • 109155
    • 109217
    • 109159
    • 109172
    • 109211
    • 109169
Amount recalled
131

This recall covers 20 products

The agency filed one notice per product. You are reading one of them; the other 19 are below.

7 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining the pivot bearing to the ceiling-mounted support to work loose or snap off, can result in severe injuries to patients and operating personnel

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

Want the full recall guide?

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Feb 9, 2021 · Data as of Sep 19, 4:51 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.