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GE Medical Systems, LLC

GE Medical Systems, LLC Recalls

All product recalls associated with GE Medical Systems, LLC.

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Recall Summary

Total Recalls

1000

Past Year

426

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 381–400 of 4598 recalls

Venue Go Models R2/R3 (GE Medical Systems) – Battery Fire Risk (2025)

Fire/Burn Risk

The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.

High

FDAMar 6, 2025Nationwide• GE Medical Systems, LLC

Venue Fit Models R3/R4 (GE Medical Systems) – Battery Fire Risk (2025)

Fire/Burn Risk

The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.

High

FDAMar 6, 2025Nationwide• GE Medical Systems, LLC

Duloxetine Capsules 20mg (Breckenridge) – Nitrosamine Impurity (2025)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

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Class II

Moderate

FDAFeb 28, 2025Nationwide• Breckenridge Pharmaceutical, Inc.

Duloxetine Capsules 60mg (Breckenridge) – Nitrosamine Impurity (2025)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Class IIModerate

FDAFeb 28, 2025Nationwide• Breckenridge Pharmaceutical, Inc.

Duloxetine Capsules 30mg (Breckenridge) – Nitrosamine Impurity (2025)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Class IIModerate

FDAFeb 28, 2025Nationwide• Breckenridge Pharmaceutical, Inc.

Volkswagen ID.4 (Volkswagen) – Gear Position Indication Fault (2025)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021-2023 ID.4, 2022-2023 Audi Q4 e-Tron, and Q4 e-Tron Sportback vehicles. The instrument panel may not properly display the transmission gear lever indicator. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 102, "Transmission Shift Lever Sequence, Starter Interlock, and Transmission Braking Effect."

High

NHTSAFeb 27, 2025Nationwide• VOLKSWAGEN

Neupogen 300mcg (Amgen) – Stability Expiration Issue (2025)

Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.

Class IIModerate

FDAFeb 27, 2025Nationwide• Amgen, Inc.

Neupogen 480mcg (Amgen) – Stability Expiration Issue (2025)

Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.

Class IIModerate

FDAFeb 27, 2025Nationwide• Amgen, Inc.

Orange EV Husk-E (Orange EV) – Rim Weight Rating Error (2025)

Orange EV is recalling certain 2023-2024 HUSK-e XP terminal trucks. The rear Gross Axle Weight Rating (GAWR) on the federal placard is incorrect and the installed tires and rims may be inadequate for the truck's intended use. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 120, "Wheels and Rims - Other Than Passenger Cars."

High

NHTSAFeb 27, 2025Nationwide• ORANGE EV

DR Field and Brush Mower – Laceration Risk (2025)

Laceration Risk

This recall involves DR Power Tow Behind Field and Brush Mowers. The black and orange tow behind mowers have the following model and serial numbers, printed on a white label that is on the front frame of the mower. "DR" is printed on the front of the mowers. Only mowers manufactured between April 1, 2024, and August 20, 2024, are included in this recall. The manufacture date is on the serial number label affixed to the rear frame of the unit and is listed in YYYYMMDD format. Model Description Serial No. Range TB21044BEN DR BRUSH MOWER PREMIER 44T 10.5 HP BS ES 3014835626 to 3015507481 TB23244BEN DR BRUSH MOWER PRO 44T 17.5 HP BS ES 3014860338 to 3015403241 TB25344BEN DR BRUSH MOWER PRO XL44T 20 HP BS ES 3014916847 to 3015451110 TB27052BEN DR BRUSH MOWER PRO MAX52T 22 HP BS ES 3014839204 to 3015534243

High

CPSCFeb 20, 2025Nationwide• DR Power Equipment, of South Burlington, Vermont, a subsidiary of Generac Power Systems Inc., of Waukesha, Wisconsin

Centricity Universal Viewer (GE Healthcare) – Security Vulnerability (2025)

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 credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.

Moderate

FDAFeb 19, 2025Nationwide• GE Healthcare

Centricity Radiology RA600 (GE Healthcare) – Security Vulnerability (2025)

Moderate

FDAFeb 19, 2025Nationwide• GE Healthcare

VERICIS Merge Cardio (Merge Healthcare) – Measurement Workflow Risk (2025)

When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

Moderate

FDAFeb 19, 2025Nationwide• Merge Healthcare, Inc.

Centricity Cardiology CA1000 (GE Healthcare) – Security Vulnerability (2025)

Moderate

FDAFeb 19, 2025Nationwide• GE Healthcare

Centricity PACS-IW (GE Healthcare) – Security Vulnerability (2025)

Moderate

FDAFeb 19, 2025Nationwide• GE Healthcare

Volkswagen GTI (Volkswagen) – Rearview Software Issue (2025)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2022-2024 Golf GTI vehicles. A software error may delay or deactivate the rearview camera image, resulting in the rearview camera image not displaying as intended. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility."

High

NHTSAFeb 19, 2025Nationwide• VOLKSWAGEN

Centricity PACS-IW (GE Healthcare) – Security Vulnerability (2025)

Moderate

FDAFeb 19, 2025Nationwide• GE Healthcare

Merge Cardio (Merge Healthcare) – Measurement Workflow Issue (2025)

Moderate

FDAFeb 19, 2025Nationwide• Merge Healthcare, Inc.

Genesis GV70 Electrified (Genesis) – Software Problem (2025)

Hyundai Motor America (Hyundai) is recalling certain Genesis 2023-2024 G80, GV80, 2025 GV70 and 2023-2025 GV70 "Electrified" vehicles. Due to a software error, the instrument panel display may fail. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 101, "Controls and Displays."

High

NHTSAFeb 19, 2025Nationwide• GENESIS

Revolution CT System (GE Medical) – Potential System Issue (2025)

GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.

Moderate

FDAFeb 18, 2025Nationwide• GE Medical Systems, LLC