FDA Enforcement Class II Ongoing

GE Healthcare Revolution Frontier, Model Numbers: 1) 5232085-213, 2) 5873009; X-ray/computed tomography system

Recall: Z-0609-2025 · Reported December 11, 2024

Enforcement

Recall Number
Z-0609-2025
Event ID
95704
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
GE Healthcare (China) Co., Ltd.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
December 11, 2024
Initiation Date
November 5, 2024
Classification Date
December 4, 2024
Address
1F-5F BLD 1, No.1 Tongji South Road, Beijing Economic-Technological Development Area, Beijing, N/A, China

Description

GE Healthcare Revolution Frontier, Model Numbers: 1) 5232085-213, 2) 5873009; X-ray/computed tomography system

Reason

GE HealthCare has become aware of a potential issue on certain Discovery, Optima, Revolution series CT systems, and certain operator console upgrades that can result in rotated CT images. Particularly with helical, cine, and cardiac (if applicable) scan modes, after the first image of an exam, each subsequent image can be rotated by an increasing amount. The amount of progressive image rotation is dependent on the gantry speed and the duration of the scan. The final image in the exam can be rotated up to a maximum of ~56 degrees. The entire anatomy rotates as a whole by equal degrees, without distortion, and the anatomical positioning and z-axis of the images remains correct. Small degrees of image rotation might not be noticed. If image rotation is noticed and necessitates a rescan of the patient, the same image rotation will reoccur.

Code Info

UDI/DI 00195278362230: 1) 5232085-213, Serial/Sales Order Numbers: CBDUG2400017HM, CBDUG2400016HM; 2) 5873009, Serial/Sales Order Numbers: CBDUG2400014HM

Distribution

Worldwide distribution.

Quantity

3 units