---
title: "GE Healthcare (China) Co., Ltd. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search GE Healthcare (China) Co., Ltd. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/ge-healthcare-china-co-ltd/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# GE Healthcare (China) Co., Ltd. recall records

**24** reported ongoing

24 records in this archive. Latest source date Jan 31, 2025.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## Records and reported status

Jan 31, 2025 FDA device enforcement

### [SIGNA Creator, SIGNA Explorer, NMRI systems](https://isitonrecall.com/recall/fda-device-z-1239-2025-signa-creator-signa-explorer-nmri-systems/)

For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by ...

Class II Reported ongoing

Distribution: Domestic US distribution nationwide. International distribution worldwide.

[Official source for SIGNA Creator, SIGNA Explorer, NMRI systems](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1239-2025%22)

Jan 31, 2025 FDA device enforcement

### [Brivo MR355, NMRI system](https://isitonrecall.com/recall/fda-device-z-1240-2025-brivo-mr355-nmri-system/)

For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by ...

Class II Reported ongoing

Distribution: Domestic US distribution nationwide. International distribution worldwide.

[Official source for Brivo MR355, NMRI system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1240-2025%22)

Jan 31, 2025 FDA device enforcement

### [Optima MR360, NMRI system](https://isitonrecall.com/recall/fda-device-z-1241-2025-optima-mr360-nmri-system/)

For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by ...

Class II Reported ongoing

Distribution: Domestic US distribution nationwide. International distribution worldwide.

[Official source for Optima MR360, NMRI system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1241-2025%22)

Jan 31, 2025 FDA device enforcement

### [SIGNA MR355, SIGNA MR360, NMRI system](https://isitonrecall.com/recall/fda-device-z-1242-2025-signa-mr355-signa-mr360-nmri-system/)

For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by ...

Class II Reported ongoing

Distribution: Domestic US distribution nationwide. International distribution worldwide.

[Official source for SIGNA MR355, SIGNA MR360, NMRI system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1242-2025%22)

Jan 31, 2025 FDA device enforcement

### [SIGNA MR380, NMRI system, Non-US Only](https://isitonrecall.com/recall/fda-device-z-1243-2025-signa-mr380-nmri-system-non-us-only/)

For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by ...

Class II Reported ongoing

Distribution: Domestic US distribution nationwide. International distribution worldwide.

[Official source for SIGNA MR380, NMRI system, Non-US Only](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1243-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Discovery RT, Model Number 2374681-17, X-ray/computed tomography systems labeled as:](https://isitonrecall.com/recall/fda-device-z-0600-2025-ge-healthcare-discovery-rt-model-number-2374681-17-x-ray-computed-tomography-systems-labeled-as/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Discovery RT, Model Number 2374681-17, X-ray/computed tomography systems labeled as:](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0600-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Optima 520, Catalog number 5439126; X-ray/computed tomography systems](https://isitonrecall.com/recall/fda-device-z-0601-2025-ge-healthcare-optima-520-catalog-number-5439126-x-ray-computed-tomography-systems/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Optima 520, Catalog number 5439126; X-ray/computed tomography systems](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0601-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Optima 680 Expert, Model number 6670000; X-ray/computed tomography system](https://isitonrecall.com/recall/fda-device-z-0602-2025-ge-healthcare-optima-680-expert-model-number-6670000-x-ray-computed-tomography-system/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Optima 680 Expert, Model number 6670000; X-ray/computed tomography system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0602-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Revolution ACE, Model number 6670000-3; X-ray/computed tomography systems](https://isitonrecall.com/recall/fda-device-z-0603-2025-ge-healthcare-revolution-ace-model-number-6670000-3-x-ray-computed-tomography-systems/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Revolution ACE, Model number 6670000-3; X-ray/computed tomography systems](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0603-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Revolution Advance, Model number 5849504; X-ray/computed tomography systems](https://isitonrecall.com/recall/fda-device-z-0604-2025-ge-healthcare-revolution-advance-model-number-5849504-x-ray-computed-tomography-systems/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Revolution Advance, Model number 5849504; X-ray/computed tomography systems](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0604-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Revolution Ascend, Model number 6969000-100; X-ray/computed tomography system](https://isitonrecall.com/recall/fda-device-z-0605-2025-ge-healthcare-revolution-ascend-model-number-6969000-100-x-ray-computed-tomography-system/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Revolution Ascend, Model number 6969000-100; X-ray/computed tomography system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0605-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Revolution Ascend Elite, Model Number 6967000-100; X-ray/computed tomography system](https://isitonrecall.com/recall/fda-device-z-0606-2025-ge-healthcare-revolution-ascend-elite-model-number-6967000-100-x-ray-computed-tomography-system/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Revolution Ascend Elite, Model Number 6967000-100; X-ray/computed tomography system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0606-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Revolution Eagle, Model Number 5849504-3, X-ray/computed tomography system](https://isitonrecall.com/recall/fda-device-z-0607-2025-ge-healthcare-revolution-eagle-model-number-5849504-3-x-ray-computed-tomography-system/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Revolution Eagle, Model Number 5849504-3, X-ray/computed tomography system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0607-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Revolution EVO, Model Number 5454001-260; X-ray/computed tomography system](https://isitonrecall.com/recall/fda-device-z-0608-2025-ge-healthcare-revolution-evo-model-number-5454001-260-x-ray-computed-tomography-system/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Revolution EVO, Model Number 5454001-260; X-ray/computed tomography system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0608-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Revolution Frontier, Model Numbers: 1) 5232085-213, 2) 5873009; X-ray/computed tomography system](https://isitonrecall.com/recall/fda-device-z-0609-2025-ge-healthcare-revolution-frontier-model-numbers-1-5232085-213-2-5873009-x-ray-computed-tomography-sy/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Revolution Frontier, Model Numbers: 1) 5232085-213, 2) 5873009; X-ray/computed tomo...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0609-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Revolution Maxima, Model Numbers: 1) 6665000-2, 2) 6670000-2, 3) 6670000-200, 4) 6670000-6; X-ray/computed tomography system](https://isitonrecall.com/recall/fda-device-z-0610-2025-ge-healthcare-revolution-maxima-model-numbers-1-6665000-2-2-6670000-2-3-6670000-200-4-6670000-6-x-ra/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Revolution Maxima, Model Numbers: 1) 6665000-2, 2) 6670000-2, 3) 6670000-200, 4) 66...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0610-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Revolution Maxima M, Model Number, 6670000-2; X-ray/computed tomography system](https://isitonrecall.com/recall/fda-device-z-0611-2025-ge-healthcare-revolution-maxima-m-model-number-6670000-2-x-ray-computed-tomography-system/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Revolution Maxima M, Model Number, 6670000-2; X-ray/computed tomography system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0611-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Revolution Maxima Select, Model Number, 6670000-55; X-ray/computed tomography system](https://isitonrecall.com/recall/fda-device-z-0612-2025-ge-healthcare-revolution-maxima-select-model-number-6670000-55-x-ray-computed-tomography-system/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Revolution Maxima Select, Model Number, 6670000-55; X-ray/computed tomography system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0612-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Operator Console Upgrade Types, FRU Spare Parts Number B79632DA: EU: RT Refresh Package, Non-EU: Discovery RT, Optima CT580, or Discovery CT590 RT; X-ray/computed ...](https://isitonrecall.com/recall/fda-device-z-0613-2025-ge-healthcare-operator-console-upgrade-types-fru-spare-parts-number-b79632da-eu-rt-refresh-package-n/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Operator Console Upgrade Types, FRU Spare Parts Number B79632DA: EU: RT Refresh Pac...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0613-2025%22)

Nov 5, 2024 FDA device enforcement

### [GE Healthcare Operator Console Upgrade Types, FRU Spare Parts Number B80212DA: EU: Operator Console (for BrightSpeed, Elite/BrightSpeed Elite Select), Non-EU: BrightSpeed Elite,...](https://isitonrecall.com/recall/fda-device-z-0614-2025-ge-healthcare-operator-console-upgrade-types-fru-spare-parts-number-b80212da-eu-operator-console-for/)

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 mod...

Class II Reported ongoing

Distribution: Worldwide distribution.

[Official source for GE Healthcare Operator Console Upgrade Types, FRU Spare Parts Number B80212DA: EU: Operator Conso...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0614-2025%22)

## Reasons in these listed records

- For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by the operator, such a...
- 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 ...

These examples come from this result page and are not a ranking of every recall reason.

## Checking GE Healthcare (China) Co., Ltd.

### Is there a recall on ge healthcare (china) co., ltd. right now?

This archive contains 24 records, including 24 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

### How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier.

### Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

### What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices.

### Where can I find older records?

Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

## Keep checking

[Search GE Healthcare (China) Co., Ltd.](https://isitonrecall.com/check/?q=GE%20Healthcare%20%28China%29%20Co.%2C%20Ltd.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
