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GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc Recalls

All product recalls associated with GE OEC Medical Systems, Inc.

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Recall Summary

Total Recalls

1000

Past Year

583

Class I (Serious)

Most Recent

Dec 2025

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 9961–9980 of 10937 recalls

GE OEC Medical Systems, Inc: GE OEC 9900 Elite Fluoroscopy System with Integrated Navi...

Missing, mixed or lost patient images may result after X-ray procedures. Error in navigation accuracy.

FDASep 13, 2006FL, GA, IL +11 more• GE OEC Medical Systems, Inc

Varian Medical Systems: GammaMed 12it radionuclide applicator system, Varian Medi...

Medical device for patient treatment does not meet electrical safety standards.

FDASep 11, 2006AZ, GA, IL +2 more• Varian Medical Systems

Varian Medical Systems: GammaMed 12i radionuclide applicator systems, distributed...

Medical device for patient treatment does not meet electrical safety standards.

FDASep 11, 2006AZ, GA, IL +2 more• Varian Medical Systems

1...497 498499500 501...547

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Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila: Abbott AxSYM Matrix Cells--Product List No: 8A73-02, sold...

Increase in complaints regarding controls out of range, calibration errors, and discrepant patient results with the AxSYM Troponin-I ADV assay.

FDASep 8, 2006Nationwide• Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila

Becton Dickinson & Company: BD Vacutainer Luer-Lok Access Device Holder with Pre-Atta...

Reports of failure of the Luer Lok Access Device to lock securely to certain catheter devices because the male luer taper surface is not within the specification.

FDASep 8, 2006Nationwide• Becton Dickinson & Company

Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila: Abbott AxSYM system FSH Master Calibrators (LN 7A60-30),...

Following a customer complaint, Abbott found an atypical stability profile for the lot of the calibrators listed in this recall. The investigation to date has shown that both controls and patient results have shifted upwards over time together.

FDASep 7, 2006PR• Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila

Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila: Architect FSH Calibrators (LN 6C24-01), for in vitro diag...

FDASep 7, 2006PR• Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila

Learn-Around Playground (LeapFrog) – arm entrapment hazard (2006)

The Learn-Around Playground is a multi-colored, plastic musical activity center for young children ages 6 to 36 months. It includes a Slide and Sing alphabet panel and a ball drop on the left side, a Number Rock musical keyboard in the center, and a Flying Rhymes airplane, pop-up LittleLeap, and "smart" book on the right side. "Leap Frog Baby" is printed on the activity center. Item number 10200 is written underneath the activity table below "Made in China."

CPSCSep 7, 2006Nationwide• LeapFrog Enterprises Inc., of Emeryville, Calif.

Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila: FSH Calibrators (LN 9C06-01), for in vitro diagnostic use.

FDASep 7, 2006PR• Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila

Diagnostic Chemicals, Ltd.: Microalbumin Multi-Calibrator Set, in vitro diagnostic. ...

Microalbumin Multi Calibrator mislabeled label on Level 5 and Level 6, cap label correct

FDASep 6, 2006Nationwide• Diagnostic Chemicals, Ltd.

Varian Medical Systems Inc: Clinac High Energy Medical Linear Accelerator, Medical Ch...

The chain holding the device gantry in position may break.

FDAAug 31, 2006Nationwide• Varian Medical Systems Inc

Medtronic Emergency Response Systems, Inc.: LIFEPAK 20 external defibrillator/monitor

Devices with v38 system software do not display a ''LOW BATTERY: CONNECT TO AC POWER'' message when the monitor is on backup (DC) battery power and may shut down without warning.

FDAAug 30, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Garden Treasures Fireplace (Agio) – fire hazard (2006)

Fire/Burn Risk

The recalled fireplace consists of a round fire bowl that rests on four legs, with a chimney cap and hood. The fireplace is made of steel and is painted black. They are about 3 feet tall and 2 feet wide. The item number, 91023, is printed on the package materials.

CPSCAug 29, 2006Nationwide• Agio International Company, Limited, of Hong Kong

Milano Counter Stools (FDL) – fall hazard (2006)

The recalled stools have four legs, are made of wood, and have dark brown or black seats. The counter stool is 24 inches tall and the bar stool is 30 inches tall. The stools have item numbers 202448 and 118136, which can be found on the packaging material.

CPSCAug 29, 2006Nationwide• FDL Inc., of Kokomo, Ind.

Nicolet Biomedical Div of Viasys Healthcare: NicoletOne version 5.20 software (also known as NicoletOn...

A software anomaly exists in the 5.20.1038 NicoletOne LTM, Sleep, nEEG, vEEG and ICU Monitor systems using the M, and/or C series amplifiers. If this anomaly occurs, the system will display the data for channel one in all channels on NicoletOne LTM, Sleep, nEEG, vEEG or ICU Monitor systems.

FDAAug 25, 2006Nationwide• Nicolet Biomedical Div of Viasys Healthcare

Philips Medical Systems North America Co. Phillips: Allura Xper FD 10 x-ray, angiographic system

Potential for x-ray system to freeze during an examination, and inability of table to be re-positioned.

FDAAug 24, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Allura Xper FD 10/10 x-ray, angiographic system

Potential for x-ray system to freeze during an examination, and inability of table to be re-positioned.

FDAAug 24, 2006Nationwide• Philips Medical Systems North America Co. Phillips

Lawnmower Blades (Blount) – replacement defect (2006)

Laceration Risk

The recalled replacement lawnmower blades are intended for use on Snapper riding lawnmowers. The recalled blades are sold for use as replacement parts under the Oregon® and Silver Streak® brands only. Original equipment blades on Snapper lawnmowers and "Snapper" brand replacement blades are not included in this recall. The recalled blades are red and marked "MADE IN USA," "GRASS SIDE CX", "Oregon" or "SILVER STREAK." The part number and date code are engraved on one side of the blade. The recalled blades are part numbers: 99-111, 99-112, 99-113, 99-114, 99-117, 99-118, 99-926, 99-930 and date codes: BL, BM, BN, BP, BQ, BR, BS, BT, BU, BV, BW, BX, BY, BZ, CA, CB, CC, CD, CE, CF, CG, CH, CJ, CK, CL, CM, CN, CP.

CPSCAug 23, 2006Nationwide• Blount International Inc., of Kansas City, Mo.

GE OEC Medical Systems, Inc: GE OEC 9800 Fluoro C-Arm X-ray System, GE OEC Medical Sys...

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

Cordless Electric Lawnmowers (Black & Decker) – fire hazard (2006)

Fire/Burn Risk

The mowers were sold under both the Black & Decker and Craftsman brand names. The recalled Black & Decker mowers have the model CMM1000 or CMM1000R and are labeled as Type 1 through Type 4, both of which are located on the silver and black label affixed to the rear door of the mower. Mowers labeled as Type 5 are not included in this recall. The Black & Decker mowers have either an orange or green deck with a black motor cover. The Craftsman brand mowers have model number 900.370520 and include all date codes and types. The model number is located on the silver and black label affixed to the rear door of the mower. The Craftsman mowers have a dark green deck with a black motor cover.

CPSCAug 16, 2006Nationwide• Black & Decker (U.S.) Inc., of Towson, Md.