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Siemens Medical Solutions USA, Inc recalls ARTIS Q, Interventional Fluroscopic x-ray system
Recalled March 29, 2017 · FDA recall Z-1534-2017 · Siemens Medical Solutions USA
Hazard
In Artis systems with A100G generators, a component can be affected by aging which could result in the potential failure of a module in the high-voltage generator. · FDA Class II
Units
264 distributed worldwide (112 in the U.S.)
Sold at
Distributed throughout the United States.
Description
In Artis systems with A100G generators, a component can be affected by aging which could result in the potential failure of a module in the high-voltage generator.
Product
ARTIS Q, Interventional Fluroscopic x-ray system
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →