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Siemens Medical Solutions USA, Inc recalls Artis icono floor-angiography systems developed for single and biplane diagnostic imaging and interventional procedures
Recalled June 15, 2022 · FDA recall Z-1246-2022 · Siemens Medical Solutions USA
Hazard
if the protective earth is interrupted and an additional fault leads to a fault current, the detection of the fault current may not be ensured may cause an electric shock if a person is in contact with metallic parts of the Carm · FDA Class II
Units
13 units
Sold at
US Nationwide distribution.
Description
if the protective earth is interrupted and an additional fault leads to a fault current, the detection of the fault current may not be ensured may cause an electric shock if a person is in contact with metallic parts of the Carm
Product
Artis icono floor-angiography systems developed for single and biplane diagnostic imaging and interventional procedures SMN: 11327700
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →