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Siemens Medical Solutions USA, Inc recalls Artis Q and Q.Zen fluoroscopic x-ray system
Recalled March 22, 2017 · FDA recall Z-1466-2017 · Siemens Medical Solutions USA
Hazard
A gap in the housing of the wireless foot switch could potentially result in liquids penetrating the interior. Such liquids may include disinfectants, cleaning agents and/ or bodily fluids. In rare cases, the introduction of liquids in the wireless foot switch housing could result in the failure of the foot switch. · FDA Class II
Units
2,158 units distributed in US and 6,139 units worldwide
Sold at
Distributed Nationwide
Description
A gap in the housing of the wireless foot switch could potentially result in liquids penetrating the interior. Such liquids may include disinfectants, cleaning agents and/ or bodily fluids. In rare cases, the introduction of liquids in the wireless foot switch housing could result in the failure of the foot switch.
Product
Artis Q and Q.Zen fluoroscopic x-ray system
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →