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Siemens Medical Solutions USA, Inc recalls Artis Q Biplane, Model No. 10848282; Artis Q Ceiling, Model No.10848281; Artis Q Floor, Model No. 10848280; Artis Q z
Recalled March 25, 2020 · FDA recall Z-1495-2020 · Siemens Medical Solutions USA
Hazard
A software issue could potentially cause the stand and table movements to be blocked. · FDA Class II
Units
1452 worldwide (638 US)
Sold at
US Nationwide distribuiton.
Description
A software issue could potentially cause the stand and table movements to be blocked.
Product
Artis Q Biplane, Model No. 10848282; Artis Q Ceiling, Model No.10848281; Artis Q Floor, Model No. 10848280; Artis Q zeego, Model No. 10848283 Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →