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Siemens Medical Solutions USA, Inc recalls Siemens Artis zee systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interv
Recalled August 12, 2015 · FDA recall Z-2340-2015 · Siemens Medical Solutions USA
Hazard
The possibility exists for a large amount of liquid to seep through the top cover of the table and penetrate the components inside the table. If this occurs, table movements may no longer be possible. No injuries reported. · FDA Class II
Units
N/A
Sold at
US Nationwide
Description
The possibility exists for a large amount of liquid to seep through the top cover of the table and penetrate the components inside the table. If this occurs, table movements may no longer be possible. No injuries reported.
Product
Siemens Artis zee systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography, general angiography, rotational angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures.
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →