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General Electric Medical Systems Information Technology

General Electric Medical Systems Information Technology Recalls

All product recalls associated with General Electric Medical Systems Information Technology.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 22061–22080 of 25002 recalls

General Electric Medical Systems Information Technology: GE ApexPro Oximeter systems (ApexPro CH or ApexPro FH wit...

Potential misuse of the ApexPro Telemetry System and incorrect message and alarm information in the ApexPro Operator's Manual may impact patient safety. When ApexPro Telemetry systems are used with SpO2 oximeters: 1. ApexPro FH Transceiver can operate with the ApexPro FH Xpod connected, but without ECG lead wires attached to the transceiver. This is unintended use of the device that is not do

FDASep 25, 2009Nationwide• General Electric Medical Systems Information Technology

Edwards Lifesciences Research Medical, Inc.: EndoClamp aortic catheter label reading in part: "CARDIOV...

Spontaneous balloon rupture during use of the product.

FDASep 24, 2009Nationwide• Edwards Lifesciences Research Medical, Inc.

Edwards Lifesciences Research Medical, Inc.: EndoClamp aortic catheter. Label reading in part: "***CAR...

Balloon catheters were spontaneously rupturing during use.

1...1102 110311041105 1106...1251

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FDASep 24, 2009Nationwide• Edwards Lifesciences Research Medical, Inc.

Parachute Hammocks (Grand Trunk) – fall risk (2009)

The recalled hammocks were sold in single and double versions and packaged in a nylon sack. The Grand Trunk logo is printed on the sack. The following models and colors are included in the recall: SH-01 (Single Olive/Khaki), SH-02 (Single Blue/Navy Blue), SH-06 (Single Royal/Khaki), DH-01 (Double Olive/Khaki), DH-02 (Double Lt. Blue/Yellow), DH-03(Double Navy/Silver), DH-04 (Double Navy/Red). The model number can be located on the product's hang tag.

CPSCSep 23, 2009Nationwide• Travel Hammock Inc., dba Grand Trunk, of Skokie, Ill.

Ventana Medical Systems Inc: VENTANA PATHWAY anti-HER-2/neu (4B5) RABBIT MONOCLONAL PR...

Incorrect result: Light staining inconsistencies with lot number 680957 of the Ventana PATHWAY HER-2/neu (4B5) Rabbit Monoclonal Primary Antibody.

FDASep 17, 2009Nationwide• Ventana Medical Systems Inc

Toshiba American Medical Systems Inc: SSH-880CV Aplio Artida System

Toshiba America Medical Systems (TAMS) is initiating a field correction on the SSH-880CV Aplio Artida System due to a problem related to a wrong measurement value display in using with DICOM viewer. When an image is transferred from this system in DICOM transfer and a measurement is performed on a Doppler image in the DICOM viewer, measured values such as VTI (Velocity Time Integral) and PI/RI

FDASep 16, 2009Nationwide• Toshiba American Medical Systems Inc

Varian Medical Systems Oncology Systems: VARiS 6.2, 6.1 and 6.0 when used with LINK, Model numbers...

Software issue: Under certain circumstances, when a therapy treatment field is transferred to VARiS Vision 6.2, 6.1 and 6.0 via LINK procedures, the rotation direction will be reversed.

FDASep 15, 2009AL, FL, IL +8 more• Varian Medical Systems Oncology Systems

Medtronic Inc. Cardiac Rhythm Disease Managment: This device is not approved in the United States. Medtron...

A subset of active implanted Concerto CRT-D and Virtuoso ICD devices worldwide (estimated at 6,300) may not meet expected device longevity due to gradually increasing current drain caused by low voltage capacitor degradation. This issue may present in the affected devices as reaching the Recommended Replacement Time (RRT) earlier than projected. This issue does not compromise device functionalit

FDASep 9, 2009ID, WY• Medtronic Inc. Cardiac Rhythm Disease Managment

Medtronic Inc. Cardiac Rhythm Disease Managment: Medtronic Virtuoso DR, D154AWG, Dual Chamber implantable ...

FDASep 9, 2009ID, WY• Medtronic Inc. Cardiac Rhythm Disease Managment

Medtronic Inc. Cardiac Rhythm Disease Managment: Medtronic Virtuoso VR, Model D154VWC, Single Chamber impl...

FDASep 9, 2009ID, WY• Medtronic Inc. Cardiac Rhythm Disease Managment

Medtronic Inc. Cardiac Rhythm Disease Managment: Medtronic Concerto, C154DWK, Dual chamber implantable car...

FDASep 9, 2009ID, WY• Medtronic Inc. Cardiac Rhythm Disease Managment

Medtronic Inc. Cardiac Rhythm Disease Managment: This device is not approved in the United States. Medtron...

FDASep 9, 2009ID, WY• Medtronic Inc. Cardiac Rhythm Disease Managment

Bicycle Chains (SRAM) – Fall Hazard (2009)

The recall involves SRAM PowerLock connector links, which are sold individually, on 10-speed bicycle chains and as original equipment on some bicycles. The recalled PowerLock connector links are identified by a date code of M or N, which is located on the side of the PowerLock connector link. 10-speed SRAM chains that were equipped with recalled PowerLock connector links include the following chain model numbers: PC-1030, PC-1050, PC-1070, PC-1090 and PC-1090R. The recalled chains were also installed on some Guru, Surly, Salsa, BMC, Serotta, Seven, and Ridley brand complete bicycles. The individual PowerLock connectors and bike chains with these connectors were sold from January 2009 through August 2009; bicycles with affected chains were sold from April 2009 through August 2009.

CPSCSep 8, 2009Nationwide• SRAM LLC, of Chicago, Ill.

Children's Animal Masks and Pendants – Lead Exposure (2009)

Fire/Burn Risk

This recall involves a children's animal mask and four styles of metal pendants. The mask resembles the face of a cat. The pendants have various animated symbols including a dog tag with fire symbol (Bleach), knife and lion symbol (Final Fantasy), Mickey Mouse symbol (Kingdom of Hearts), and a burning sun symbol (Naruto). The pendants were sold with silver-colored chains.

CPSCSep 8, 2009Nationwide• Team Work Trading, of Los Angeles, Calif.

Sigma-Aldrich Mfg LLC: Sigma-Aldrich Histopaque-1077, Ref. 10771, packaged in 50...

Some of the product was contaminated with Pseudomonas mendocina

FDASep 4, 2009Nationwide• Sigma-Aldrich Mfg LLC

Medical Components, Inc dba MedComp: Medcomp, 10F Bioflex Tesio Kit with cutting trocar. Catal...

mislabeled as right are actually left

FDASep 2, 2009Nationwide• Medical Components, Inc dba MedComp

Greatbatch Medical: Enpath Lead Adapter, Ref: 501214. The contents of the in...

The silicone tubing of affected leads was processed outside of validated parameters. Although the material remains biocompatible, test data regarding the performance characteristics are not available.

FDASep 1, 2009CA, MN• Greatbatch Medical

Hitachi Medical Systems America Inc: Hitachi Oasis Magnetic Resonance Scanners Software V1.0C ...

The device has a software error that could potentially lead to a misdiagnosis.

FDASep 1, 2009Nationwide• Hitachi Medical Systems America Inc

Greatbatch Medical: Enpath Myopore Sutureless Myocardial Pacing Lead, Ref: 5...

FDASep 1, 2009CA, MN• Greatbatch Medical

Smoothtop Electric Ranges (Frigidaire) – Fire Hazard (2009)

Fire/Burn Risk

This recall involves Frigidaire, Frigidaire Gallery, Frigidaire Professional and Kenmore Elite smoothtop electric ranges with rotary knobs and digital displays. The following model and serial numbers are included in the recall: Frigidaire (Serial Number Range VF122xxxxx - VF831xxxxx) and Models Beginning with FEFBZ90GC FEFLMC55GC FEFLZ87GC GLEF396AB GLEF396AQ GLEF396AS GLEF396CQ GLEF396CS GLEFM397DB GLEFM397DQ GLEFM397DS GLEFM97FPB GLEFM97FPW GLEFM97GPB GLEFM97GPW LEEFM389FE PLEF398AC PLEF398CC PLEF398DC PLEFM399DC PLEFMZ99EC PLEFMZ99GC PLEFZ398EC PLEFZ398GC Kenmore Elite (Serial Number Range VF122xxxxx - VF334xxxxx) and Models Beginning with 790.99012 790.99013 790.99014 790.99019 The model and serial number can be found by opening the range drawer at the base of the unit.

CPSCAug 27, 2009Nationwide• Frigidaire, a division of Electrolux Home Products Inc., of Augusta, Ga.