FDANovember 30, 2020device

Artis zee/ zeego & Artis Q/ Q.zen Artis Pheno

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

When the user changes frame rates from lower frequency (e.g. 10 f/s) to higher frequency (e.g. 30 f/s) during continuous release of Fluoro "Fluoro Override", the measured Air Kerma Rate can exceed the regulatory limits.

What to do

FDA enforcement status: Ongoing

Brands named

siemens medical solutionssiemenssiemens medical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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