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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

276

Class I (Serious)

242

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 3781–3800 of 4099 recalls

General Electric Medical Systems Information Technology: GE Healthcare CIC Pro Clinical Information Center, Centra...

Two separate issues may occur with operating The CiC Pro v4.1 System with Telemetry. 1) Experience a loss of audible alarms when operating system memory resource reaches approximately 170MG. This will occur if CIC Pro continuously runs for average of 160 day, and 2) System may continuously reboot upon start up in an attempt to correct the issue.

FDAJan 24, 2007DE, HI, ID +6 more• General Electric Medical Systems Information Technology

General Electric Medical Systems Information Technology: GE Healthcare CIC Pro Clinical Information Center, Centra...

Alarm and Reboot problems: Two separate issues could occur with the CIC Pro system when used with Telemetry. Each issue occurs in software version v4.1 only; A) the system may experience a loss of audible alarms when operating system memory resources reach 170MB and/or B) the system may intentionally or unexpectedly reboot .

FDAJan 24, 2007Nationwide• General Electric Medical Systems Information Technology

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Boston Scientific Corporation One Boston: HTA Console System, 230 Volt , French, Product Number: 5...

Defective integrated circuit board could result in loss of the system pump and patient injury (hot fluid 90 degree C into uterus) if in use during the recirculation/heating phase of treatment

FDAJan 24, 2007Nationwide• Boston Scientific Corporation One Boston

Boston Scientific Corporation One Boston: HTA Console System, 110 Volt, Product Number: 56000 (HT...

Defective integrated circuit board could result in loss of the system pump and patient injury (hot fluid 90 degree C into uterus) if in use during the recirculation/heating phase of treatment

FDAJan 24, 2007Nationwide• Boston Scientific Corporation One Boston

Catch Incorporated: Homocysteine Reagent Test Kit. The Homocysteine test ki...

A high homocysteine level can be reported as falsely low.

FDAJan 18, 2007CA, PA• Catch Incorporated

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation; for diagnostic ima...

The Centricity PACS RA1000 Workstation Software may manifest certain mammography image display problems only if the images were acquired through GE Senographe versions 2000D, DS or Essential.

FDAJan 12, 2007Nationwide• GE Healthcare Integrated IT Solutions

Advanced Neuromodulation Systems, Inc: Eon Rechargeable Implantable Pulse Generator (IPG) System

Product's external charging system on occasion was failing to communicate with the Implantable Pulse Generator preventing re-charging of the pain relief system.

FDADec 22, 2006Nationwide• Advanced Neuromodulation Systems, Inc

Integrated Orbital Implants Inc: Perry-Kolberg Titanium Motility/Support System (Threaded ...

The threads on the threaded sleeve were manufactured with left-handed threads, requiring a modification to the surgical technique for proper insertion. Failure to properly identify the affected components and apply the modified insertion technique will result in an inability to insert the sleeve into the implant.

FDADec 20, 2006Nationwide• Integrated Orbital Implants Inc

Boston Scientific Corporation One Boston: Wallstent Endoscopic Biliary Endoprosthesis- 8mm x 40mm, ...

Guidewire restriction during use (excessive adhesive in the guidewire lumen)

FDADec 20, 2006Nationwide• Boston Scientific Corporation One Boston

International Technidyne Corp.: International Technidyne Corporation (ITC) ProTime Microc...

Incorrect Test Results-ProTime ITC''s Microcoagulation System: Professional Instrument may report incorrect test results when more than 50 tests are in the memory and the technician uses the AUTO Send or PRINT RESULTS feature.

FDADec 6, 2006Nationwide• International Technidyne Corp.

K-GUARD Fire Extinguishers (Ansul) – Potential Failure (2006)

Fire/Burn Risk

The recall involves K-GUARD® Wet Chemical, FLAG FIRE® KITCHEN ONE® Wet Chemical, FLAG FIRE® Water and SENTRY® Water Fire Extinguishers manufactured and shipped between May 2003 and September 9, 2005. The recall program involves pick-up tube replacements in the following extinguishers: Brand Model Part Number(s) K-GUARD® Wet Chemical K01-1 430849 (UL) 430850 (ULC) K01-2 432843 (UL) 432848 (ULC) SENTRY® Water W02-1 430847 (English) 430848 (Spanish/English) FLAG FIRE® KITCHEN ONE® Wet Chemical KS-6000 552055 (UL) 552500 (ULC) FLAG FIRE® Water PWS-25G 552050 (UL) 552501 (ULC) Model numbers can be found on the fire extinguisher labels. Affected models meet the following criteria: The year 2004 or 2005 is stamped on the hanger hook attachment on the shell. For 2003 models, information on specific serial numbers included in the recall can be found at www.ansul.com for the K-GUARD Wet Chemical and SENTRY Water extinguishers, or at www.pyrochem.com for the FLAG FIRE and KITCHEN ONE Wet Chemical extinguishers. Contact the firm to determine if your extinguisher is included in this replacement program.

CPSCNov 13, 2006Nationwide• Ansul Incorporated, of Marinette, Wis.

Atrium Medical Corporation: Atrium Express Dry Seal Chest Drain with Sterile Fluid Pa...

Chest drainage tubing incorrectly assembled and may disconnect from patient during use

FDANov 8, 2006Nationwide• Atrium Medical Corporation

Data Innovations, Inc.: Roche Cobas driver (rchcob6i), analytical laboratory data...

Software of modular driver may incorrectly report patient results as Quality Control Results

FDANov 3, 2006Nationwide• Data Innovations, Inc.

Data Innovations, Inc.: Roche Modular Drive (rchmdlri), analytical laboratory dat...

Software of modular driver may incorrectly report patient results as Quality Control Results

FDANov 3, 2006Nationwide• Data Innovations, Inc.

Edwards Lifesciences Corporation of Puerto Rico: Edwards Lifesciences VANTEX Central Venous Catheter Set w...

Lack of Assurance of Sterility-Device packaging was manufactured with an incorrect lid that could compromise the sterility of the product.

FDANov 2, 2006Nationwide• Edwards Lifesciences Corporation of Puerto Rico

Goulds Pump Products – Fire Suppression Fault (2006)

Fire/Burn Risk

The recalled pumps are general in purpose, but are sometimes used in fire suppression systems. The pumps were sold under the Goulds Pumps, Bell & Gossett and Red Jacket Water Products brands. The pumps can be identified by having Model NPE, NPO, MCC, MCS, SM or Series 3530 on their nameplate. Recalled pumps were manufactured between December 2005 and September 7, 2006. They have date code M05, A06, B06, C06, D06, E06, F06, G06, H06 or J06. The date code is the first three digits of the serial number on the pump nameplate.

CPSCOct 25, 2006Nationwide• ITT Water Technology Inc., of Auburn, N.Y.

Quechua Tents and Canopies (Decathlon) – Flammability Risk (2006)

Fire/Burn Risk

All 2006 model Quechua branded tents (2-Seconds, 2-Seconds Air, 3-Seconds Air, T2, T3 Air, T4 Air, T6.2XL Air, T2 Ultralight Tents, T0 and T0+ canopies) sold in orange, red, blue, camouflage, or beige with SKU numbers 350808, 65196, 86813 146552, 146548, 100986, 351219, 370833, 531980, 531989, 65024, 90366, 90428, 567008, 567009, 567036, 567032, 370973, 22611, 566985, and 566992 are included in this recall. The SKU number can be found on the self-carry jacket. Quechua is printed on the exterior of the tent or canopy and on some of the carrying bags.

CPSCOct 17, 2006Nationwide• Decathlon USA, of Wilmington, Mass.

ARC Bicycle Light Batteries (Light & Motion) – Fire Risk (2006)

Fire/Burn Risk

The recalled batteries are found in Light & Motion 2004 ARC Li-Ion HID lighting systems. The lights are black with "ARC" and "LIGHT & MOTION" written in yellow letters. The recall includes only batteries with a manufacturer date code of 1003 or 1103. The date code is stamped on the bottom of the battery and "LIGHT & MOTION" is printed on the side of the battery.

CPSCOct 17, 2006Nationwide• GP Batteries International Ltd., of Singapore

Matrix Distributors, Inc.: One Touch Ultra Blood Glucose Test Strips-Lot # 2691191, ...

Counterfeit Test Strips (manufacturer unknown)

FDAOct 9, 2006Nationwide• Matrix Distributors, Inc.

Arctic Cat Snowmobile – Steering Failure (2006)

Fire/Burn Risk

The recalled steering shafts were installed on the following models: All 2002 440 Sno Pro Models All 2003 Firecat 500/600/700, Firecat 700 Sno Pro, and 440 Sno Pro Models All 2004 Firecat 500/600/700 (STD and Sno Pro), and Sabercat 500/600/700 Models All 2005 Firecat 500/600/700 (STD and Sno Pro), M5,M6,M7, and Sabercat 500/600/700 Models All 2006 Crossfire 600/700, Firecat 500/600/700, Firecat 700 Sno Pro, Sabercat 500/600/700, and all M-Series

CPSCSep 19, 2006Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.