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Siemens Medical Solutions USA, Inc recalls CIOS ALPHA; image intensified fluoroscopic x-ray system

Recalled November 4, 2015 · FDA recall Z-0118-2016 · Siemens Medical Solutions USA

Hazard
patient procedure interruption due to a potential system failure · FDA Class II
Units
44
Sold at
Nationwide Distribution.

Description

patient procedure interruption due to a potential system failure

Product
CIOS ALPHA; image intensified fluoroscopic x-ray system
Manufacturer(s)
Siemens Medical Solutions USA, Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Siemens Medical Solutions USA, Inc recalls CIOS ALPHA; image intensified fluoroscopic x-ray system | RecallWatchUSA