ProductGuru Recalls

Official recall record

GE Healthcare Discovery RT, Model Number 2374681-17, X-ray/computed tomography systems labeled as:

US FDA — Medical Devices · 2024-11-05 · ChinaClass II
Issuing authority
US FDA — Medical Devices
Alert date
2024-11-05
Country of alert
China
Alert level
Class II
Alert type
recall
Barcode (EAN/GTIN)
00840682118699
Brand on record
GE Healthcare (China) Co., Ltd.

What the authority reported

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.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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