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GE Medical Systems Information Technologies

GE Medical Systems Information Technologies Recalls

All product recalls associated with GE Medical Systems Information Technologies.

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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 3601–3620 of 3680 recalls

GE Medical Systems Information Technologies: GE Medical Systems COROMETRICS Maternal/Fetal Monitoring ...

The 2120 Main Board on device lacks required external safety 'watchdog' circuit.

FDAMay 21, 2003CA, IN, MD +5 more• GE Medical Systems Information Technologies

Merit Medical Systems, Inc: Inject 10 Coronary Control Syringe (CCS), 10ml

Cracks in the syringe barrels could allow for air aspiration into the syringe barrel.

FDAMay 16, 2003Nationwide• Merit Medical Systems, Inc

Merit Medical Systems, Inc: Custom Kit

Cracks in the syringe barrels could allow for air aspiration into the syringe barrel.

FDAMay 16, 2003Nationwide• Merit Medical Systems, Inc

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Misys Healthcare Systems: Misys Laboratory System, version 5.3

Two clients reported Quality Assurance dates could not be entered after 5/19/03.

FDAMay 13, 2003Nationwide• Misys Healthcare Systems

GE OEC Medical Systems, Inc: Uroview 2000 X-ray System

Uncommanded motion of the urological table is possible should the hand control assembly be exposed to liquids.

FDAMay 12, 2003Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: Uroview 2500 X-ray System

Uncommanded motion of the urological table is possible should the hand control assembly be exposed to liquids.

FDAMay 12, 2003Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: Uroview 2600 Uroview System

Uncommanded motion of the urological table is possible should the hand control assembly be exposed to liquids.

FDAMay 12, 2003Nationwide• GE OEC Medical Systems, Inc

Fujifilm Medical System USA, Inc.: Synapse Version 2.2.1 and 2.3.1 software

Synapse Version 2.2.1 and 2.3.1 Software [Free-Hand Region] may lead to incorrect density calculations during CT scan

FDAMay 12, 2003Nationwide• Fujifilm Medical System USA, Inc.

Ventana Medical Systems Inc: iVIEW DAB Detecion Kit. Catalog Number 760-091

Kit does not stain tissues properly.

FDAMay 7, 2003Nationwide• Ventana Medical Systems Inc

System 02 Inc 1090 Upper Hembree Rd Roswell GA 300761140: Rejuv O2 Home Oxygen Spa 98% + Pure, Non-pressurized Oxy...

System 02 oxygen flow rate found to be inadequate and Rejuv02 Home Oxygen Bar contains 'Adulterated Labeling.'

FDAMay 1, 2003GA, IN• System 02 Inc 1090 Upper Hembree Rd Roswell GA 300761140

System 02 Inc 1090 Upper Hembree Rd Roswell GA 300761140: System O2, Portable Humidified Oxygen Delivery System Ove...

System O2 oxygen flow rate found to be inadequate and RejuvO2 Home Oxygen Bar contains 'Adulterated Labeling.'

FDAMay 1, 2003GA, IN• System 02 Inc 1090 Upper Hembree Rd Roswell GA 300761140

GE Medical Systems Information Technologies: Power cord manufactured by ElectriCord Manufacturing Comp...

Reports of broken plug ground pins on AC power cords for patient monitors.

FDAApr 30, 2003Nationwide• GE Medical Systems Information Technologies

Stryker Howmedica Osteonics: Trident Insert Impactor

The ball retaining sleeve on the Trident Insert Impactor can possibly disassemble.

FDAApr 28, 2003IN• Stryker Howmedica Osteonics

Vellux Fahrenheit Electric Blankets - Temperature Malfunction (2003)

Fire/Burn Risk

The Vellux® fahrenheit™ blankets were sold in various colors and sizes to fit all mattress sizes. The temperature controller is white, with the words "WESTPOINT STEVENS" and "fahrenheit Heated Blanket" printed on the front. The recall includes blankets manufactured from July 2002 through January 2003. The manufacture date is printed on a label sewn into the seam.

CPSCApr 24, 2003Nationwide• WestPoint Stevens Inc., of West Point, Ga.

Steris Corp: C1140 Flexible Endoscope Processing Container and Tray as...

The container flow port is inverted, which restricts the flow of sterilant to the endoscope and affects the sterilization process.

FDAApr 23, 2003Nationwide• Steris Corp

Steris Corp: C1141 Flexible Endoscope Processing Container, designed ...

The container flow port is inverted, which restricts the flow of sterilant to the endoscope and affects the sterilization process.

FDAApr 23, 2003Nationwide• Steris Corp

Philips Medical Systems (Cleveland) Inc: Intinion 1.5 T MRI Scanner.

There is a potential for the patient to be exposed to cryogenic fluids (liquid air) dripping from the vent during a quench due to the location of the vent.

FDAApr 17, 2003Nationwide• Philips Medical Systems (Cleveland) Inc

General Electric Medical Systems Information Technology: MAC-LAB 3000EX systems

There is an incorrect jumper set-up on a motherboard of the devices that could eventually cause a polyfuse to overheat resulting in smoke.

FDAApr 14, 2003Nationwide• General Electric Medical Systems Information Technology

General Electric Medical Systems Information Technology: MAC-LAB (Classic) systems

There is an incorrect jumper set-up on a motherboard of the devices that could eventually cause a polyfuse to overheat resulting in smoke.

FDAApr 14, 2003Nationwide• General Electric Medical Systems Information Technology

Misys Healthcare Systems: Misys Laboratory System versions 5.2, 5.23, 5.3, 5.3.1 an...

Incorrect results could be filed.

FDAApr 14, 2003Nationwide• Misys Healthcare Systems