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GE Healthcare, LLC recalls Proteus XR/a (SlOK : K993090)
Recalled October 2, 2019 · FDA recall Z-2449-2019 · GE Healthcare
Hazard
Intermittently not receiving an audible exposure indication upon completion of an exposure on the Proteus stationary radiographic system. · FDA Class II
Units
647 US; 167 OUS
Sold at
Worldwide - US Nationwide
Description
Intermittently not receiving an audible exposure indication upon completion of an exposure on the Proteus stationary radiographic system.
Product
Proteus XR/a (SlOK : K993090)
Manufacturer(s)
GE Healthcare, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →