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Siemens Medical Solutions USA, Inc recalls Artis Zee Angiographic x-ray systems.
Recalled April 9, 2014 · FDA recall Z-1309-2014 · Siemens Medical Solutions USA
Hazard
An inappropriate cable connection was assembled for certain Artis zee systems. which may cause a system failure and possibly lead to a restricted maneuverability of the gantry system. · FDA Class II
Units
9
Sold at
MN, WI, PA, MI, AL, OH, NC, AR, and NJ.
Description
An inappropriate cable connection was assembled for certain Artis zee systems. which may cause a system failure and possibly lead to a restricted maneuverability of the gantry system.
Product
Artis Zee Angiographic x-ray systems.
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →