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…
Read the official notice →- Date
- 2025-04-09
- Country
- United States
- Brand
- GE Healthcare
- Product
- GE Healthcare Centricity Centricity PACS-IW with Universal Viewer, Model Numbers: 1) 2049587-015; 2) 2066908-086; 3) 2066908-136; 4)…
- Classification
- Class II
- Units
- Worldwide distribution.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More GE Healthcare recalls
- 2026-04-08
USGE 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.
- 2025-03-05
- 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.
Other drugs & medical recalls in the United States
- 2025-04-09
- US
Draeger, Inc. recalls Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable Product Description:…
The potential for cracks forming in the breathing circuit hose.
FDA · DeviceDraeger, Inc.Domestic: Nationwide Distribution. International - following countries:…Official notice → - US
Terumo Cardiovascular Systems Corporation recalls Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe, Catalog Number REF CD1754
During some clinical cases, it has been observed that the SO2 value may periodically appear as dashes on the Touchscreen Display indicating unavailable data. In these cases, a yellow low-limit alarm will also be…
FDA · DeviceTerumo Cardiovascular Systems CorporationUS: IL, TX, NY, MI, FL, NV, and Australia, New ZealandOfficial notice → - US
Stryker Spine recalls Monterey AL Implant Inserter; 14/16mm; Catalog 48019120.
Potential for the gold unlock button to separate from the inserter.
FDA · DeviceStryker SpineDomestic: CA, CO, FL, GA, IL, MA, NE, NH, NY, OK, PA, TX, UT. International:…Official notice → - US
Stryker Corporation recalls Otopore Cylinder outer ear wound dressing, Firm Catalog Number 5400-020-000 and Forte Catalog Number 5400-020-000TL
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
- US
Glenmark Pharmaceuticals Inc., USA recalls chlorproMAZINE Hydrochloride Tablets, USP 100 mg, Rx Only, 100 Tablets per bottle, Manufactured for: Glenmark Pharmaceuticals…
CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit.
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Breckenridge Pharmaceutical, Inc. recalls Duloxetine Delayed-Release Capsules, USP, 30 mg, Rx Only, 1,000 Capsules per bottle, Manufactured by: Towa Pharmaceutical…
CGMP Deviations: presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the recommended interim limit.