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Siemens Medical Solutions USA, Inc recalls Axiom Artis systems. C-arm angiographic x-ray system x-ray, angiographic system.

Recalled September 4, 2013 · FDA recall Z-2108-2013 · Siemens Medical Solutions USA

Hazard
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. · FDA Class II
Units
178
Sold at
US Distribution including the states of PA, NJ, DC, VA, MD and DE.

Description

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.

Product
Axiom Artis systems. C-arm angiographic x-ray system x-ray, angiographic system.
Manufacturer(s)
Siemens Medical Solutions USA, Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Siemens Medical Solutions USA, Inc recalls Axiom Artis systems. C-arm angiographic x-ray system x-ray, angiographic system. | RecallWatchUSA