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GE Medical Systems, LLC

GE Medical Systems, LLC Recalls

All product recalls associated with GE Medical Systems, LLC.

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Recall Summary

Total Recalls

1000

Past Year

582

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 8961–8980 of 10937 recalls

GE Medical Systems, LLC: Innova 3100/3100IQ GE Innova 3100 / 3100 IQ, Cardiovascul...

GE Healthcare has recently became aware of a potential power supply failure with the Innova 2000, 3100 and 4100 systems that may impact patient safety. A potential power supply failure inside the GE equipment cabinet could occur with no advance warning and thereby prevent x-ray generation and image processing. Should this occur, the system cannot be restarted.

FDAJul 31, 2009AL, AZ, AR +39 more• GE Medical Systems, LLC

SWR Natural Blonde Acoustic Bass Amplifiers (Fender) – fire hazard (2009)

Fire/Burn Risk

The recall involves the SWR® Natural Blonde™ 120V acoustic bass amplifier, model 44-60600-000. The amplifier measures about 26 inches x 16 inches x 15 inches, and has a blonde-textured vinyl covering with a black control plate and black stamped steel vibration-free grill. The model number is located on the top rear panel of the amplifier. "SWR" and "Natural Blonde" are printed on the front of the amplifier.

CPSCJul 31, 2009Nationwide• Fender Musical Instruments Corp. (FMIC), of Scottsdale, Ariz.

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Linvatec Corp. dba ConMed Linvatec: PRO5100, PowerPro Battery Modular Handpiece. Drill mode ...

There is a potential the devices may self activate for their PowerPro, PowerProMax, and MPower I Handpieces manufactured prior to June 1, 2008.

FDAJul 31, 2009Nationwide• Linvatec Corp. dba ConMed Linvatec

Linvatec Corp. dba ConMed Linvatec: Arthro-Knife, ConMed, Linvatec 11311 Concept Blvd, Largo ...

ConMed has determined there is a possibility that the device may not fully retract once it is deployed.

FDAJul 31, 2009Nationwide• Linvatec Corp. dba ConMed Linvatec

Linvatec Corp. dba ConMed Linvatec: ST ULTRAPOWER DIAMOND WHEEL (RED) 25.4mm, Catalog Number...

ConMed Linvatec is recalling Ultrapower Bur, Diamond Wheel for possibility of a packaging breach in the sterile barrier.

FDAJul 31, 2009Nationwide• Linvatec Corp. dba ConMed Linvatec

Linvatec Corp. dba ConMed Linvatec: PowerProMax PRO5100M Battery Single Trigger, PowerProMax...

There is a potential the devices may self activate for their PowerPro, PowerProMax, and MPower I Handpieces manufactured prior to June 1, 2008.

FDAJul 31, 2009Nationwide• Linvatec Corp. dba ConMed Linvatec

GE Medical Systems, LLC: GE Medical Systems, COMPAX 40E X-ray Systems, Models; 220...

GE Healthcare has recently become aware that table lock safety features, which are provided with Compax 40E X-ray systems, are not always being utilized and has resulted in unintended lateral tabletop movement that may impact patient safety.

FDAJul 30, 2009AL, AK, AZ +43 more• GE Medical Systems, LLC

Draeger Medical Systems, Inc.: Heater Elements for Resuscitaire Infant Radiant Warmers m...

Spark, flame and smoke: A mis-positioned crimp on heater element lead wire resulted in flame and smoke aerating from the top of the warmer assembly.

FDAJul 29, 2009Nationwide• Draeger Medical Systems, Inc.

Enviro-Flo Plus Fuel Containers (Blitz USA) – fire hazard (2009)

Fire/Burn Risk

The recall involves green Enviro-Flo Plus spouts used with 1 and 2 gallon fuel containers. Only spouts with manufacture date codes listed from 04/17/2009 through 04/19/2009 are included in the recall. The manufacture date code is etched into the side of the spout. The spouts were used on fuel containers with item numbers 81005 (1-gallon) and 81010 (2-gallon) printed on the labels. Date codes affected include: 041709xx1 (April 17, 2009, Automated Assembly) 041809xx1 (April 18, 2009, Automated Assembly) 041909xx1 (April 19, 2009, Automated Assembly) All spout delivery systems manufactured outside these dates or with number sequence ending in a zero (0) are not included in this recall.

CPSCJul 28, 2009Nationwide• Blitz USA Inc., of Miami, Okla.

Medtronic Xomed, Inc.: Repose G2 Bone Screw, Sterile, REF 76310200, Lot # 62450...

Medtronic Xomed, Inc. is recalling the Repose Bone Screw System product and Bone Screw product due to improper labeling. The labeling for the Repose System was inadvertently placed on the Repose Screw and vice versa.

FDAJul 27, 2009Nationwide• Medtronic Xomed, Inc.

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

Medtronic has detected a specific pattern of MOSFET IC malfunctions in its Concerto, Virtuoso and EnRhythm family of devices. The probability of occurrence decreases with time and, to date over 90% of the malfunctions related to the pattern have occurred within the first twelve months after implant.

FDAJul 27, 2009Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Virtuoso DR, Model D154AWG, Dual Chamber implan...

FDAJul 27, 2009Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Xomed, Inc.: Repose G2 Bone Screw System, Sterile, REF 76353200; Lot #...

FDAJul 27, 2009Nationwide• Medtronic Xomed, Inc.

Sevylor Tow Behinds – connector break risk (2009)

The recall involves the following model Sevylor® Tow Behinds with Quick Hitch component. The Quick Hitches were manufactured between 2005 and 2009. Model No. Description 2000002098 Avenger ST2467 Daytona U362YEL Daytona U346RED Devil Ray ST9007 Double Threat U350BLK Double Threat U350GRN Double Threat ST2607 Drag'n Master U363RED Drag'n Master ST9401 Flight Blaster U338RED Flight Blaster ST2000 Le Biscuit U371RED Le Biscuit ST2540 Raging Racer U382PUR Raging Racer ST2650 Super Blaster U384BLU Super Blaster U384RED Super Blaster ST9300WM Triple Blaster ST9300 Triple Threat U351RED Triple Threat ST9050 Twin Blaster U349YEL Twin Blaster ST9075 Velocity Blaster U353YEL Velocity Blaster ST2467WM Wake Zone U362CMB Wake Zone

CPSCJul 23, 2009Nationwide• Shanghai Suofeng Plastic Metal Manufactures Co., Ltd., China

My Pal Scout Electronic Plush Toy Dogs (LeapFrog) – choking hazard (2009)

Choking Hazard

This recall involves My Pal Scout, a green and beige electronic plush dog with plastic decals on its paws. When those decals are pushed, the dog plays songs, speaks and barks. "Scout" is printed on the dog tag at the dog's neck. The plush dog measures about 9 inches high by 9 inches wide. "LeapFrog Ent. Item No. 19142" is printed on the white tag attached to the dog and on the toy's packaging. My Pal Scout dogs with embroidered paws are not included in this recall.

CPSCJul 23, 2009Nationwide• LeapFrog Enterprises Inc., of Emeryville, Calif.

Newport Medical Instruments Inc: Newport HT50 Ventilator, Model # HT-50-H, HT50-HB, HT50-H...

The recall was initiated because Newport Medical has confirmed that the HT50 Dual Pac Ventilator is not compatiable with the external battery pack (p/n BAT3300A) supplied with the previous single battery ventilator. The Dual Pac system has a slightly higher amperage draw than the single battery and as a result can cause the fuse in the external battery pack to blow making the battery inoperable.

FDAJul 22, 2009Nationwide• Newport Medical Instruments Inc

Polaris ATVs (Polaris) – fire hazard (2009)

Fire/Burn Risk

This recall involves the Polaris ATVs with model year 2009. The ATVs were sold under market names Sportsman ESP XP 850 and Sportsman XP 850 ATVs. The model and serial number identification decal is located on the left side of the machine on the frame rail below the front fender. The following models are being recalled: Market Name Model Number Sportsman ESP XP 850 A09ZX85AG Sportsman XP 850 A09ZN85AL Sportsman ESP XP 850 A09ZX85AL Sportsman XP 850 A09ZN85AQ Sportsman ESP XP 850 A09ZX85AQ Sportsman XP 850 A09ZN85AS Sportsman ESP XP 850 A09ZX85AR Sportsman XP 850 A09ZN85AT Sportsman ESP XP 850 A09ZX85AS Sportsman XP 850 A09ZN85AX Sportsman ESP XP 850 A09ZX85AX Sportsman XP 850 A09ZN8XAL Sportsman ESP XP 850 A09ZX8XAG Sportsman XP 850 A09ZN8XAQ Sportsman ESP XP 850 A09ZX8XAL Sportsman XP 850 A09ZN8XAS Sportsman ESP XP 850 A09ZX8XAQ Sportsman XP 850 A09ZN8XAX Sportsman ESP XP 850 A09ZX8XAR Sportsman ESP XP 850 A09ZX8XAS Sportsman ESP XP 850 A09ZX8XAX

CPSCJul 22, 2009Nationwide• Polaris Industries Inc., of Medina, Minn.

Elliptical Cross Trainers (Stamina) - Safety Instructions (2009)

This recall includes the following elliptical machines: Model Serial Number Magnetic 1772 Cross Trainer Elliptical Model No. 55-1772 08AUG000001-08AUG000360 08AUG000361-08AUG001078 08AUG002521-08AUG002878 08SEP001081-08SEP001438 08SEP001441-08SEP001798 08SEP002881-08SEP003238 08OCT001801-08OCT002158 08OCT002161-08OCT002518 08DEC003241-08DEC003598 Air 1725 Elliptical Cross Trainer Model No. 55-1725 08AUG000001-08AUG000596 08NOV000597-08NOV001192 09JAN000001-09JAN000596 Air Resistance 1723 Cross Trainer Model No. 55-1723 07SEP000001-07SEP001192 07OCT001193-07OCT001788 07DEC001789-07DEC002384 08JAN000001-O8JAN000596 08AUG000597-08AUG001192 08NOV001193-O8NOV001788 08DEC001789-08DEC002384 09JAN000001-09JAN000596 09MAR000597-09MAR001192 09MAY001193-09MAY001788

CPSCJul 21, 2009Nationwide• Stamina Products Inc. of Springfield, Mo.

Boston Scientific CRM Corp: Boston Scientific COGNIS CRT-D, Cardiac Resynchronization...

Laceration Risk

Boston Scientific Cardiac Rhythm Management retrieved devices that could be subject to a potential for acute non-secure lead connections when implanted. Nonsecure lead connections can manifest as high impedance, or lead electrogram artifacts resulting in oversensing and/or inappropriate delivery of therapy.

FDAJul 20, 2009AZ, CA, CT +18 more• Boston Scientific CRM Corp

Boston Scientific CRM Corp: Boston Scientific TELIGEN, Implantable Cardiac Defibrilla...

Laceration Risk

FDAJul 20, 2009AZ, CA, CT +18 more• Boston Scientific CRM Corp