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General Electric Med Systems LLC

General Electric Med Systems LLC Recalls

All product recalls associated with General Electric Med Systems LLC.

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Recall Summary

Total Recalls

1000

Past Year

426

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 4341–4360 of 4598 recalls

General Electric Med Systems LLC: Sopha Medical Vision DST / DST-XL Digital vatiable angle ...

Cracked welds on the main rotation shaft could potentially lead to the collapse of the gantry yokes that support the detectors if the system is continued to be used after the weld has completely fractured.

FDASep 27, 2005AL, AZ, CA +19 more• General Electric Med Systems LLC

Medtronic Emergency Response Systems, Inc.: standard (hard) paddles used with the LIFEPAK 12 defibril...

Potential for voltage pins in connector of therapy cable to break.

FDASep 2, 2005Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: QUIK-COMBO pacing/defibrillation/ECG (therapy) cables use...

Potential for voltage pins in connector of therapy cable to break.

FDA

1...216 217218219 220...230

Page 218 of 230Next

Sep 2, 2005

Nationwide

• Medtronic Emergency Response Systems, Inc.

Medtronic Cardiac Surgery Technologies: Medtronic SPYDER Anastomotic Device. Sterilized using ir...

Customers stated that the U-Clip deployment collar was either difficult to rotate or 'locks up' during usage, which prevents the deployment of the U-Clips.

FDASep 1, 2005Nationwide• Medtronic Cardiac Surgery Technologies

GE Medical Systems, LLC: GE Signa Advantage nuclear magnetic resonance imaging sys...

During use of GE Signa nuclear magnetic resonance imaging system, a flexible Teflon tube that was part of the magnet vent system ruptured and allowed the magnet to vent into the scan room. Because of helium pressure inside the room, the scan room door could not be reopened after the patient was removed from the scan room.

FDAAug 19, 2005Nationwide• GE Medical Systems, LLC

Datex Ohmeda, Inc. dba GE Healthcare: Ohmeda Giraffe SPOT PT Lite Phototherapy System

Phototherapy medical device may lose its position and can cause a safety hazard to the patient.

FDAAug 5, 2005IN• Datex Ohmeda, Inc. dba GE Healthcare

Inogen, Inc: Portable Oxygen Generator

Firm plans to upgrade all units to correct situations that could lead to interuption in oxygen delivery.

FDAAug 1, 2005Nationwide• Inogen, Inc

Boehringer Laboratories, Inc.: Boehringer Suction Regulator Model number 3704

Condition exists that prevents complete shutoff of the valve

FDAAug 1, 2005AK, AZ, CA +12 more• Boehringer Laboratories, Inc.

Angiomed Gmbh Wachhausstrasse 6 Karlsruhe Germany: Bard Luminexx Endoscopic Biliary Stent and Delivery Syste...

Biliary Stents may malfunction and cause failure to expand, fracture, incomplete deployment, inaccurate positioning, migration, or lumen perforation.

FDAJul 28, 2005Nationwide• Angiomed Gmbh Wachhausstrasse 6 Karlsruhe Germany

GE Medical Systems Information Technologies: GE Healthcare Centricity Cardiology AI1000 Workstation ve...

The potential exists for the AI1000 workstation to mix images from one study with images from another study. Mixed studies could be from the same patient or from different patients. Mixed patient images could compromise patient condition or diagnosis and treatment.

FDAJul 18, 2005AL, AZ, AR +38 more• GE Medical Systems Information Technologies

Medtronic Emergency Response Systems, Inc.: Hard shell carry case for the LIFEPAK 500 AED.

Some hard shell carry case for LIFEPAK 500 and LIFEPAK CR Plus automated external defibrillators may have blocked pressure vent which may make it difficult to open the case after a sudden decrease in altitude (such as in aircraft landng or mountain descent).

FDAJul 12, 2005Nationwide• Medtronic Emergency Response Systems, Inc.

Bicycle Wheels (Rolf Prima) – Rear Wheel Failure (2005)

These 2003 Rolf Prima Vigor and Elan wheels were sold in a front and rear wheel set. Only the rear wheel is affected. "Rolf Prima Vigor" or "Rolf Prima Elan" are written on the wheel rim. The wheel models have serial numbers between 03926 and 06586. The serial number is located on the rim, under the yellow rim tape and is not visible from the outside of the wheel. The tire, tube and rim strip must be removed.

CPSCJul 6, 2005Nationwide• Rolf Prima Inc., of Eugene, Ore.

Guidant Cardiac Surgery: Aortic Cutter, single use device consisting of grip, cutt...

Laceration Risk

Incomplete or no aortotomy may occur with use of the aortic cutter on unaltered tissue, or incomplete aortotomy may result when the cutter is used on altered tissue. Use of the cutter on altered tissue has caused the aortic plug to not be captured by the device

FDAJul 5, 2005FL, MO, NE +1 more• Guidant Cardiac Surgery

Medtronic Neurosurgery: Medtronic Neurosurgery C/N 3805-014 Peelaway Introducer S...

Cracked hubs/handles and/or improper peeling of the sheath during use.

FDAJul 5, 2005Nationwide• Medtronic Neurosurgery

Birch and Bark Candles (Target) – Potential Hazard (2005)

Fire/Burn Risk

The recalled candles were sold individually wrapped in a ribbon on a plate. This recall also includes candles sold in boxed sets of three candles under the Restore & Restyle brand. The candles are cream in color and were sold in sizes 3 by 3 inches, 3 by 6 inches, 4 by 6 inches and 6 by 6 inches.

CPSCJun 24, 2005Nationwide• Target Corp., Minneapolis, Minn.

Spinning Water Teethers (Prestige) – Child Safety Risk (2005)

Choking Hazard

The water-filled teether is bright green or blue with a green and blue plastic butterfly or turtle in the center, which spins around. The spinner contains small beads, which produce a rattling sound. They have Style #47447 (butterfly) and #47448 (turtle) written on the packaging.

CPSCJun 23, 2005Nationwide• Prestige Toy Corp., of New York, N.Y.

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

The defibrillator may not operate if the device is turned on during an AC Loss Alert.

FDAJun 17, 2005Nationwide• Medtronic Emergency Response Systems, Inc.

GVP Ceramic Hair Straightening Iron (Generic Value Products) – Fire Risk (2005)

Fire/Burn Risk

This hair straightening iron has a black housing with golden-colored ceramic heating plates. "Generic Value Products™" is written on the top of the iron and "GVP™" is written in a white circle on the side of the iron. The iron was packaged in a black and white box with the letters GVP™ in large type in the upper left hand front corner. The SKU is 264800, which is written on the packaging.

CPSCJun 2, 2005Nationwide• Generic Value Products, of Omaha, Neb.

Carter Brothers Fun-Kart Go-Kart – Safety Issue (2005)

The recall includes one-seater models 1136-3020, 1136-3021, 1136-3420, 1136-3421, 1205-3020 and two-seater models 2336-3021, 2336-3022, 2336-5019, 2575-3020, 2575-3420, 2605-3416, 2605-3515, 2606-3016, 2606-3017, 2606-3416, 2606-3417, 2636-3016, 2636-3017, 2906-3015, 2906-3016, 2906-3017, 2906-4015, 2906-4016, 2906-4017, 2909-3015, 2909-3415, 2909-4015, 2910-3015, 2910-3016, 2910-3415, 2910-4015, 2910-4016, 2910-4415, 2911-4015, 2911-4016, 2946-3015, and 2946-3016. The model number and serial number are located under the seat (on the driver's side if two-seater). The Fun-Karts were produced in several colors, to include red, black, blue, purple and green.

CPSCMay 20, 2005Nationwide• Carter Brothers Manufacturing Co. Inc., of Brundidge, Ala.

Theragenics Corporation: PG910 Spacers, Part number SP101, loaded into Bard Expres...

The spacers loaded in the seeding cartridges were expired and/or the extra loose spacers were labeled with an incorrect expiration date.

FDAMay 16, 2005OH, VA• Theragenics Corporation