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GE Healthcare, LLC recalls Revolution CT ES - Product Usage: intended for head, whole body, cardiac and vascular X-ray Computed Tomography applicat
Recalled December 30, 2020 · FDA recall Z-0694-2021 · GE Healthcare
Hazard
A potential for protocol(s) with unintended patient orientation or scan setting when using Intelligent Protocoling · FDA Class II
Units
2 units
Sold at
Worldwide distribution - US Nationwide distribution including in the states of FL and TX. The countries of Belgium, France, and Spain.
Description
A potential for protocol(s) with unintended patient orientation or scan setting when using Intelligent Protocoling
Product
Revolution CT ES - Product Usage: 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 →