GE Healthcare recalls
41 official recalls and safety alerts involving GE Healthcare since 2021-10, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with GE Healthcare or the relevant agency.
- 2026-09-23
USGE Healthcare recalls Centricity PACS Server V7, intended for managing digital medical images and associated data, All versions
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient…
- 2026-04-08
- US
GE Healthcare LLC recalls SIGNA Premier systems
Whole-Body MR scanners used to produce images of the inside of the human body to aid diagnosis of disease may have been manufactured/serviced with ferrous (steel) fittings instead of non-ferrous (brass) fittings on the…
FDA · DeviceGE Healthcare LLCWorldwide - US Nationwide distribution in the states of CA, MA, NJ, NY, OH,…Official notice → - 2026-03-11
- US
GE Healthcare recalls GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: 2110344-039, 2110344-046, 2110344-047; System, Image…
Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP) with versions ZFP v6.0: SP11.6, SP11.6.0.1 and SP11.6.1 on…
FDA · DeviceGE HealthcareWorldwide distribution - US Nationwide and the countries of Belarus, Brazil,…Official notice → - 2025-12-24
- US
GE Healthcare GmbH recalls GE HealthCare ViewPoint 6, Catalog Number H47601AA; Radiological image processing system
GE HealthCare has become aware that the Patient History tab in ViewPoint 6 versions 6.15.3 and 6.15.4 ultrasound software may not include complete patient medical history information.
- 2025-04-09
- US
GE Healthcare recalls GE Healthcare Centricity Centricity PACS-IW with Universal Viewer, Model Numbers: 1) 2049587-015; 2) 2066908-086; 3) 2066908-136; 4)…
There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login…
- 2025-03-05
- US
GE Healthcare (China) Co., Ltd. recalls 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…
FDA · DeviceGE Healthcare (China) Co., Ltd.Domestic US distribution nationwide. International distribution worldwide.Official notice → - 2024-12-11
- US
GE Healthcare (China) Co., Ltd. recalls 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,…
- 2024-12-04
- US
GE Healthcare (China) Co., Ltd. recalls GE Proteus XR/A radiographic system
Steel cables in the Wall Stand for certain Proteus XR/a systems serviced by GE HealthCare have not been replaced at the intervals detailed in the Preventative Maintenance Action List.
- 2024-11-13
- US
GE Healthcare recalls GE Healthcare Centricity Universal Viewer Zero Footprint, Model Numbers: 1) 2089507-083, GDZH-JINWAN-Centricity 2) 2089507-093,…
GE HealthCare has become aware of an issue in Centricity Universal Viewer Zero Footprint Client (ZFP) where there is a potential security vulnerability which could allow a malicious actor to access the system and…
FDA · DeviceGE HealthcareWorldwide distribution - United States Nationwide and the countries of…Official notice → - 2024-10-16
- US
GE Healthcare recalls GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model/Catalog/Code Numbers: a)¿¿¿¿¿ 2089507-120; b)¿¿¿¿ 2089507-129;…
GE HealthCare has become aware of an issue in Centricity Universal Viewer Zero Footprint Client (ZFP) version v6.0 SP11.x where the latest report is not shown by default to the user. The issue may occur when a study…
- 2024-10-02
- US
GE Healthcare recalls GE Healthcare Centricty PACS, V2, V3, V4, V6, V7; Radiological imaging processing system.
GE HealthCare has become aware of an issue where image storage is not possible when Centricity PACS reaches the maximum number of unique image identifiers (Ckeys). If this occurs, it can result in acquisition of a…
- 2024-09-25
- US
GE Healthcare recalls GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: a) 2110344-008; b) 2110344-009; c) 2110344-010; d)…
Footprint Client (ZFP) versions v6.0 SP9.x and SP10.x where the latest addended report is not shown by default to the user. The issue occurs when the addendum is created on the same day as the original report but at a…
- US
GE Healthcare GmbH recalls ViewPoint 6, Model Numbers: a) H47581RJ, b) H47591MA, c) H47591MT, d) H47591PE, e) H47591PR, f) H47591RA, g) H47591SD, h) H47591YA;…
The National Institute of Standards and Technology (NIST) has identified in the National Vulnerability Database (NVD) that NexGen Healthcare Mirth Connect, prior to version 4.4.1, has a potential vulnerability allowing…
FDA · DeviceGE Healthcare GmbHUS Nationwide distribution including in the states of Alabama, Alaska,…Official notice → - 2024-09-04
- US
GE Healthcare (China) Co., Ltd. recalls GE Healthcare Proteus XR/a, stationary X-Ray System, Model/Catalog Numbers: 1) 2259973; 2) 2259988; 3) 2266999; 4) 2373519; 5)…
The XR system, Proteus XR/a, does not have a de-installation manual describing process steps for de-installing the devices. De-installation instruction process steps must be followed when de-installing these devices to…
- 2023-11-01
- US
GE Healthcare recalls Universal Viewer Workflow Manager, Image processing radiological system
When using Universal Viewer or Centricity Universal Viewer with Workflow Manager (WFM), if a third-party reporting application is used to launch exams, it could display information on a different patient than WFM and…
FDA · DeviceGE HealthcareNationwide distribution to AR, AZ, CA, CO, DE, FL, GA, IL, IN, ME, MI, MN, MO,…Official notice → - US
GE Healthcare recalls Centricity PACS-IW with Universal Viewer, versions 5.0 SPx with PACS-IW foundation; Radiological Image Processing System
GE HealthCare has become aware of an issue where images from two different patients may be contained in a single study, when stored in Centricity PACS-IW V3.7.x, Centricity PACS-IW with Universal Viewer V5.0 and…
FDA · DeviceGE HealthcareUS and Austria, Azerbaijan, Bosnia and Herzegovina, Brazil, Canada, Chile,…Official notice → - 2023-05-10
- US
GE Healthcare recalls Centricity PACS-IW with Universal Viewer, Model/Catalog Numbers: a) 2066908-061, b) 2066908-077, c) 2066908-086, d) 2066908-111, e)…
GE HealthCare has become aware of an issue where information from two different patients can be mismatched when correcting patient or study information.
- 2022-08-31
- US
GE Healthcare, LLC recalls (1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX; (3) GE Universal…
Inaccurate Distance and Area measurements with use of Global Stack viewport.
FDA · DeviceGE Healthcare, LLCDistribution was made to AR, AZ, CA, CO, DE, FL, GA, IA, ID, IL, IN, KS, LA,…Official notice → - 2022-08-17
- US
GE Healthcare, LLC recalls Service manuals for the CT, PET, or NM table as follows: GT1700/GT1700V/VT1700, GT2000/VT2000, GT2000x/VT2000x, High Capacity Table, Lite…
As a result of unclear guidance in the service manual, the table can drop during a specific service activity if the wrong screws are removed by the service personnel without the appropriate table supports in place…
FDA · DeviceGE Healthcare, LLCUS Nationwide distribution including PR. There was also government/military…Official notice → - 2022-08-03
- US
GE Healthcare, LLC recalls Centricity PACS Software Version 7.0 SP0.0.4.7
The Event Notification Manager (ENM) functionality for certain products does not process notifications for study modifications performed on post verified exams.
FDA · DeviceGE Healthcare, LLCWorldwide distribution - US Nationwide distribution in the states of CO, NV,…Official notice → - 2022-07-27
- US
GE Healthcare, LLC recalls SIGNA Premier magnetic resonance scanner, model 5748519.
Under rare conditions, SIGNA Premier gradient coils could result in elevated acoustic noise during scanning. After prolonged periods of elevated acoustic noise, this could potentially lead to hearing loss.
FDA · DeviceGE Healthcare, LLCWorldwide distribution - US Nationwide distribution in the states of AL, AZ,…Official notice → - US
GE Healthcare, LLC recalls GE Healthcare Avance CS2, Avance CS2 Pro Anesthesia Systems, Part #1009-9050-000; and Aisys CS2 Anesthesia Systems, Part # 1011-9050-000.
The base of the anesthesia system can have a crack and could potentially fracture resulting in a tip or overbalance of the anesthesia system. This can result in potential injury if it falls on a person.
FDA · DeviceGE Healthcare, LLCDistribution was made to AZ, CA, CO, CT, FL, IA, ID, IL, IN, KY, LA, MA, MD,…Official notice → - US
GE Healthcare, LLC recalls GE Healthcare Aisys CS2 Anesthesia System, Part number 1011-9050-000; and Avance CS2 and Avance CS2 Pro Anesthesia System, Part number…
There is a potential reversal of the O2 and air cylinder pressure transducer connections.
FDA · DeviceGE Healthcare, LLCWorldwide Distribution. US nationwide, Australia, Austria, Belgium, Bolivia,…Official notice → - 2022-07-13
- US
GE Healthcare, LLC recalls GE Centricity Universal Viewer Zero Footprint. To view, communicate, process, and display Medical images and data within a computer…
Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP)
- 2022-07-06
- US
GE Healthcare, LLC recalls Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured on or after April 1, 2019
Backup batteries can fail earlier than their estimated life.
FDA · DeviceGE Healthcare, LLCWorldwide distribution - US Nationwide and the countries of Algeria,…Official notice → - 2022-06-22
- US
GE Healthcare, LLC recalls CARESCAPE Central Station (CSCS) V2, Model numbers 2082278-001 and 2082279-001. Update 3/10/2023: The following FRU and display part…
The CARESAPE Central Station (CSCS) V2 can shut down due to a potential power supply component failure. This can lead to loss of patient monitoring at the central station.
FDA · DeviceGE Healthcare, LLCWorldwide distribution - US Nationwide. There was also military/government…Official notice → - 2022-06-15
- US
GE Healthcare, LLC recalls Centricity Radiology RA600
Potential for Distance and Area measurements to display inaccurate measurement values when performed on magnified images, and specific to ZFP, Distance and Area measurements can display inaccurate measurement values…
FDA · DeviceGE Healthcare, LLCWorldwide distribution. Nationwide distribution to AL, AR, AZ, CA, CO, CT, DC,…Official notice → - US
GE Healthcare, LLC recalls Replacement back up batteries distributed on or after April 1, 2019, for CARESCAPE R860, Engstr¿om Carestation and Engstr¿om PRO…
Insufficient battery backup power resulting in premature shutdown of the ventilator when not connected to AC mains power supply.
FDA · DeviceGE Healthcare, LLCWorldwide Distribution: US (nationwide) to AL, AR, AZ, CA, CO, CT, FL, GA, HI,…Official notice → - 2022-04-27
- US
GE Healthcare, LLC recalls GE Healthcare MR Systems, Magnetic Resonance imaging (MRI). SIGNA Premier, SIGNA Architect, SIGNA Pioneer, Discovery MR750w 3.0T,…
During the de-installation of an MR system magnet, if all rigging and hardware that attach to the magnet for transportation are not properly installed and secured, the magnet may fall, leading to potential injury.
FDA · DeviceGE Healthcare, LLCWorldwide Distribution: US (nationwide), including Puerto Rico and the U.S.…Official notice → - 2022-04-20
- US
GE Healthcare, LLC recalls MUSE Cardiology Information System, Model Numbers: a) 3101011-040, b) 3101010-401, c) 3101010-009, d) 3101010-008
Two scenarios may cause edits to measurements and diagnosis statements can be lost after a test is Signed in the MUSE NX web client.
FDA · DeviceGE Healthcare, LLCUS and Australia, Austria, Bahrain, Belgium, Brazil, Canada, Denmark, England,…Official notice → - 2022-04-13
- US
GE Healthcare, LLC recalls Signa 1.5T TwinSpeed Magnetic Resonance Imaging System
There is potential for the images to be flipped left to right.
FDA · DeviceGE Healthcare, LLCWorldwide Distribution. US nationwide, Argentina, Australia, Azerbaijan,…Official notice → - US
GE Healthcare, LLC recalls Revolution Apex, Revolution CT with Apex Edition
The accumulated dose is incorrectly displayed in certain situations. There are two situations that will result in the SmartStep displayed dose being inaccurately high.
- 2022-03-23
- US
GE Healthcare, LLC recalls GE Healthcare CARESCAPE Central Station (CSCS) V2.0x MAI700 (Integrated), REF 2082278-001, and MAS700 (Desktop, REF 2082279-001.
If the CARESCAPE Central Station v2.0 is used with an unapproved keyboard, the audio can be muted resulting in loss of audible alarms.
FDA · DeviceGE Healthcare, LLCWorldwide distribution - US nationwide, including Puerto Rico. There was also…Official notice → - 2022-02-16
- US
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Artist system, nuclear magnetic resonance imaging system.
The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
FDA · DeviceGE Healthcare, LLCDistribution was nationwide, including Puerto Rico and the Virgin Islands.…Official notice → - 2022-02-02
- US
GE Healthcare, LLC recalls GE Vscan Extend, being sold as "Vscan Extend Sector DICOM"
The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connected to a computer without AC power.
FDA · DeviceGE Healthcare, LLCDomestic: AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY,…Official notice → - 2021-12-08
- US
GE Healthcare, LLC recalls GE Centricity Universal Viewer Zero Footprint Client
There is a potential to display incomplete patient imaging study.
FDA · DeviceGE Healthcare, LLCWorldwide distribution - US Nationwide distribution in the states of AR, AZ,…Official notice → - 2021-12-01
- US
GE Healthcare, LLC recalls Computed Tomography Systems Revolution CT, Revolution CT ES, Revolution Apex, Revolution CT with Apex edition
The accumulated dose is incorrectly displayed in certain situations. Thisoccurs during an interventional exam using the SmartStep option if the table height is adjusted after the exam starts. In this situation, the…
- 2021-10-27
- US
GE Healthcare, LLC recalls SIGNA Pioneer nuclear magnetic resonance imaging system
Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.
FDA · DeviceGE Healthcare, LLCDistribution in United States to AZ, CA, FL, GA, IL, LA, MA, MD, MN, NC, NH,…Official notice → - 2021-10-13
- US
GE Healthcare, LLC recalls Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system
A software anomaly exists in the Centricity Universal Viewer study management feature in which study changes are not propagated to either the Centricity Enterprise Archive (EA) or another Vendor Neutral Archive (VNA).
FDA · DeviceGE Healthcare, LLCAR, IL, ME, MS, NE, NJ, NY, and TN Belgium, Canada, Costa Rica, France,…Official notice → - 2021-10-06
- US
GE Healthcare, LLC recalls Flow sensors that may be installed in the following GEHC anesthesia machines: (1) Aestiva MRI, GTIN 0080682102339; (2) Aestiva 7900; (3)…
The flow sensors built prior to June 2021 could have damaged tubes with small punctures or cuts that could cause leaks resulting in incorrect anesthesia machine tidal volumes potentially leading to over-delivery of…
FDA · DeviceGE Healthcare, LLCDistribution was nationwide, including PR. Foreign distribution was made to…Official notice → - US
GE Healthcare, LLC recalls AMX Navigate Mobile X-Ray System
An unexpected column motion while attempting to park the column on the AMX Navigate mobile X-ray system.