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Siemens Medical Solutions USA, Inc recalls Artis zee and Artis zeego systems. x-ray, angiographic system
Recalled October 1, 2014 · FDA recall Z-2569-2014 · Siemens Medical Solutions USA
Hazard
There is a potential problem with Artis zee and Artis zeego systems running software version VC21B and being used in conjunction with the Large Display, in that under certain circumstances, the release of radiation can become blocked unnecessarily. · FDA Class II
Units
206
Sold at
Nationwide Distribution
Description
There is a potential problem with Artis zee and Artis zeego systems running software version VC21B and being used in conjunction with the Large Display, in that under certain circumstances, the release of radiation can become blocked unnecessarily.
Product
Artis zee and Artis zeego systems. x-ray, angiographic system
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →