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GE Healthcare, LLC recalls Revolution CT scanners Product Usage: The system is intended for head, whole body, cardiac and vascular X-ray Comput
Recalled July 24, 2019 · FDA recall Z-1951-2019 · GE Healthcare
Hazard
Additional low dose radiation exposure. · FDA Class II
Units
857 (US = 195: OUS = 662)
Sold at
Worldwide - US Nationwide Distribution
Description
Additional low dose radiation exposure.
Product
Revolution CT scanners Product Usage: The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications.
Manufacturer(s)
GE Healthcare, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →