Reported Jul 10, 2024 · Ongoing

ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and…

Siemens AG/Siemens Healthcare GmbH

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 AG/Siemens Healthcare GmbH · Rittigfeld 1 · Forchheim, N/A · N/A

Is this the product you have?

  • 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

3 of 3 products

Products covered by this recall
Model / numberBarcodesProduct as published
113276004056869063317ARTIS icono ceiling
113281004056869295923ARTIS icono floor
113277004056869149325
Amount recalled
201 units in total

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration. If the described issue occurs, the applied radiation dose rate may be higher than intended by the user.

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

Data as of Sep 19, 6:59 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.