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Siemens Medical Solutions USA, Inc recalls Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number: 10094137
Recalled May 5, 2021 · FDA recall Z-1495-2021 · Siemens Medical Solutions USA
Hazard
Some Artis zee ceiling systems show an increased abrasion of the cabling at the cable outlet of the inner C-arm, the limited functionality may not be sufficient to continue with treatment as planned. This may result in a situation where it is necessary to cancel clinical treatment or to continue treatment on an alternative system. · FDA Class II
Units
772 units U.S.
Sold at
Nationwide
Description
Some Artis zee ceiling systems show an increased abrasion of the cabling at the cable outlet of the inner C-arm, the limited functionality may not be sufficient to continue with treatment as planned. This may result in a situation where it is necessary to cancel clinical treatment or to continue treatment on an alternative system.
Product
Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number: 10094137
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →