PlainRecalls
FDA Devices Moderate Class II Terminated

Revolution CT with Apex Edition CT System - Product Usage: intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications.

Reported: December 30, 2020 Initiated: November 23, 2020 #Z-0695-2021

Product Description

Revolution CT with Apex Edition CT System - Product Usage: intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications.

Reason for Recall

A potential for protocol(s) with unintended patient orientation or scan setting when using Intelligent Protocoling

Details

Recalling Firm
GE Healthcare, LLC
Units Affected
3 units
Distribution
Worldwide distribution - US Nationwide distribution including in the states of FL and TX. The countries of Belgium, France, and Spain.
Location
Waukesha, WI

Frequently Asked Questions

What product was recalled?
Revolution CT with Apex Edition CT System - Product Usage: intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications.. Recalled by GE Healthcare, LLC. Units affected: 3 units.
Why was this product recalled?
A potential for protocol(s) with unintended patient orientation or scan setting when using Intelligent Protocoling
Which agency issued this recall?
This recall was issued by the FDA Devices on December 30, 2020. Severity: Moderate. Recall number: Z-0695-2021.