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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

353

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 301–320 of 3680 recalls

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

CDI OneView Monitoring System (Terumo) – Display Value Issue (2025)

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 triggered to the user, due to the dashed-out value.

Low

FDAMar 3, 2025FL, IL, MI +3 more• Terumo Cardiovascular Systems Corporation

Spectral CT on Rails (Philips) – Software Scanning Problems (2025)

Multiple problems identified with the software version leading to various scanning and image issues, and unintended device movement.

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Moderate

FDAFeb 28, 2025MN• Philips Medical Systems Nederland B.V. Veenpluis

Curtain Airbag Inflator (Key Safety Systems) – Ignition Holder Issue (2025)

Key Safety Systems, Inc. - (DBA Joyson) is recalling one side curtain air bag, part number 2009086-3. The ignition holder in the side curtain air bag may detach during air bag deployment.

High

NHTSAFeb 24, 2025Nationwide• KEY SAFETY SYSTEMS

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

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

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

Moderate

FDAFeb 18, 2025Nationwide• GE Medical Systems, LLC

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

Moderate

FDAFeb 18, 2025Nationwide• GE Medical Systems, LLC

Modular Stem (Waldemar Link) – Carton Label Error (2025)

A problem was discovered during the scanning process of the outer carton label because of an incorrect GTIN on the label, which is a GTIN for a different product.

Low

FDAFeb 14, 2025Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Sodium Chloride Injection (Nephron) – Potential Leakage (2025)

Lack of Assurance of Sterility: There is a potential for leakage at the IV bottle port.

Class IIModerate

FDAFeb 10, 2025Nationwide• Nephron Sterile Compounding Center LLC