Reported Sep 4, 2013 · Terminated

Axiom Artis systems. C-arm angiographic x-ray system x-ray, angiographic system.

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 · 51 Valley Stream Pkwy · Malvern, PA · 19355

Is this the product you have?

  • Axiom Artis systems. C-arm angiographic x-ray system x-ray, angiographic system.
Lot codes and dates
  • Multiple Model numbers
    • 10281163
    • 10281013
    • 10280959
    • 10272410
    • 10094200
    • 10094142
    • 10094141
    • 10094139
    • 10094137
    • 10094135
    • 10093961
    • 10093902
    • 8890415
    • 8890407
    • 8627718
    • 8395431
    • 8395415
    • 8395399
    • 8395381
    • 7728392
    • 7555373
    • 755365
    • 7555357
    • 7412807
    • 7151066
    • 7008605
    • 5904441
    • 5904433
    • 5895003
    • 475525
    • 475517
    • 475509
Amount recalled
178

Where it was sold

Why it was recalled

The firm became aware of a potential issue with Axiom Artis systems installed by a third party installer that may involve incorrect channel nuts being used.

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

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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 6, 2014 · Data as of Sep 19, 5:25 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.