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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

1000

Class I (Serious)

127

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 23221–23240 of 25000 recalls

General Electric Med Systems LLC: GE Healthcare Innova 3100/ 3100 IQ Digital Fluoroscopic...

Measurement errors during the computation of vessel diameters while using the Stenosis Analysis software (also known as Quantitative Coronary Analysis function-QCA) using the auto-calibration function on Innova Digital (located in control room) or in-room InnovaCentral/Touch-Screen

FDAMar 26, 2007AZ, CA, CO +22 more• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Innova 2100 IQ Digital Fluoroscopic Imagin...

FDAMar 26, 2007AZ, CA, CO +22 more• General Electric Med Systems LLC

Philips Medical Systems North America Co. Phillips: Practix 160 Mobile X-ray systems. The systems are used i...

X-ray systems lack product report certification demonstrating compliance, and were illegally introduced into the United States commerce.

1...1160 116111621163 1164...1250

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FDAMar 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Practix 300 Mobile X-ray systems. The systems are used i...

X-ray systems lack product report certification demonstrating compliance, and were illegally introduced into the United States commerce.

FDAMar 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Practix 33 Mobile X-ray systems. The systems are used in...

X-ray systems lack product report certification demonstrating compliance, and were illegally introduced into the United States commerce.

FDAMar 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

GE OEC Medical Systems, Inc: GE OEC, InstaTrak 3500 Plus FluoroTrak and Fluoro CAT Spi...

Tracking Accuracy - Image intensifier supplier's change on the C-Arm could lead to patient injury, due to incorrect anatomical location of the instrument during a procedure.

FDAMar 23, 2007AZ, CA, FL +17 more• GE OEC Medical Systems, Inc

Front Loading Washing Machines (Maytag/Samsung) – Fire Hazard (2007)

Fire/Burn Risk

The recall involves certain Maytag- and Samsung-brand front-load washers. The Maytag washers have model numbers beginning with MAH9700 or MAH8700. The Samsung model number WF306BHW or a model number beginning with WF316. Not all serial numbers are subject to the recall. The model and serial numbers are located on a tag at the bottom of the door opening. Maytag models with a serial number ending in the last two letters identified below are subject to the recall: 2005 GA GC GE GG GJ GL GN GP GR GT GV GX 2006 JA JC JE JG JJ JL JN Sample Maytag Serial Number: 10123456GN Samsung models with the six-digit number 100001 through 799999 prior to a letter at the end of the serial number are subject to the recall: Sample Samsung Serial Number: 230854AL300026B

CPSCMar 21, 2007Nationwide• Samsung Electronics Co. Ltd., of South Korea

Electronic Musical Keyboards (Casio) – Fire Risk (2007)

Fire/Burn Risk

This recall involves model CTK-710 of the Casio® 61-key full-size electronic musical keyboards. The size of the keyboard is 37-11/16 inches by 14-1/16 inches by 5-1/4 inches. Products with serial numbers ranging from 7030001 through 7040400 and 7041901 through 7043500 are included in this recall. The brand and model information are found on the front of the unit above the keyboard and the serial number is found inside the battery compartment located on the underside of the unit.

CPSCMar 20, 2007Nationwide• Casio Computer Co. Ltd., of Tokyo, Japan

St Jude Medical CRMD: St. Jude Medical-CPS Direct SL- slittable CRT lead delive...

Device Separation- product may separate at the mapping collar transition joint located at the proximal (light blue) marker band end of the tool during the implant procedure.

FDAMar 20, 2007AZ, CA, FL +20 more• St Jude Medical CRMD

Laars Boilers and Water Heaters – Carbon Monoxide (2007)

This recall involves Laars 9600 CB Condensing Heating Boilers and Laars 9600 HWG Condensing Water Heaters with black vent pipe/tubing. The recalled boilers are used to generate hot water for heating systems including baseboards or radiant flooring. The recalled water heaters generate hot water for use in homes, such as showers, sinks and dishwashers. "Mark II" and "9600 CB" or "9600 HWG" are printed on the front of the boilers and water heaters. The model number and BTU size are printed on the right side of the unit. The recalled boiler and water heater exteriors are putty and black-colored or taupe and black-colored. Only the following models are included in this recall. Model Input (Btu/h) Gas Boilers: CB 150 150,000 CB 175 175,000 CB 200 200,000 Water Heaters: HWG 150 150,000 HWG 175 175,000 HWG 200 200,000

CPSCMar 19, 2007Nationwide• Laars Heating Systems Co., of Rochester, N.H.

Philips Medical Systems North America Co. Phillips: Philips Collimators, Model numbers: 9896 010 00614, 9896 ...

The Collimator field-defining light beam does not meet the light field contrast ratio requirement of 4:1. System is non-compliant with performance standard (1020.31 (d)(2)(iii) 21 CFR

FDAMar 15, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Amprobe Digital Clamp Meters – Shock Risk (2007)

Fire/Burn Risk

Only Amprobe brand digital clamp meter models ACD-10PRO, ACD-10 TRMS-PRO, ACD-14 and ACD-14TRMS, except those model numbers followed by "FX" or "PLUS," are included in the recall. "Amprobe" and the model numbers are printed on the front of the units. These clamp meters measure 0 to 600 volts alternating current (VAC), and 0 to 600 volts direct current (VDC). In addition, they measure 0 to 400 amps alternating current. The tester body is red and gray and measures 7-1/2 inches in length by 2-1/2 inches in width by 1-1/4 inches thick.

CPSCMar 15, 2007Nationwide• Amprobe Test Tools, of Everett, Wash.

Varian Medical Systems Oncology Systems: FramelessArray software, Version 1.0. ; Medical Device fi...

Localization error; with planning data transferred to the Optical Guidance Platform via DICOM RT; The software incorrectly computes the center of the CT volume, resulting in a potential axial error ranging from 0.3 mm to 1.5 mm, affecting both Fractionated and Stereotactic Radiosurgery (SRS) Treatments

FDAMar 14, 2007IN• Varian Medical Systems Oncology Systems

Elite Operations Toy Sets – Safety Risks (2007)

Laceration Risk

This recall involves three styles of "Elite Operations" brand toy sets. The military-style play sets contain light and sound vehicles, action figures and accessories. Models included in this recall are: Super Rigs Transport Vehicle (Item # 087286), Command Patrol Center (Item # 920625) and Troop Carrier (Item # 773967). The item numbers are located on the back of the packaging above the barcode. Toy sets sold prior to January 2006 are not included in this recall. No other "Elite Operations" brand toys are affected by this recall.

CPSCMar 13, 2007Nationwide• Toy Century Industrial Company Ltd., of Hong Kong

BioHorizons Implant Systems Inc One Perimeter Park South: BioHorizons 0.035 Hex Driver, REF 300-377, BioHorizons Im...

Premature wear; The material from which the hex driver was made was improperly hardened during manufacturing and could lead to premature wear.

FDAMar 12, 2007Nationwide• BioHorizons Implant Systems Inc One Perimeter Park South

BioHorizons Implant Systems Inc One Perimeter Park South: BioHorizons 0.050 Hex Driver, Regular, REF 300-350, BioHo...

Premature Wear; The material from which the hex driver was made was improperly hardened during manufacturing and could lead to premature wear.

FDAMar 12, 2007Nationwide• BioHorizons Implant Systems Inc One Perimeter Park South

BioHorizons Implant Systems Inc One Perimeter Park South: BioHorizons 0.050 Hex Driver, Long, REF 300-351, BioHoriz...

Premature Wear; The material from which the hex driver was made was improperly hardened during manufacturing and could lead to premature wear.

FDAMar 12, 2007Nationwide• BioHorizons Implant Systems Inc One Perimeter Park South

Varian Medical Systems Inc: LINAC Scapel Treatment Planning System, incorporating Fas...

A software anomaly in a medical device used for patient treatment could result in accidental or unintended exposure radiation exposure. The tilt rotation compensation algorithm does not adequately compensate for the tilt rotation.

FDAMar 9, 2007Nationwide• Varian Medical Systems Inc

Roche Molecular Systems, Inc.: AmpliChip CYP450 Test, CE-IVD, M/N: 4381866190, Roche Mol...

The current package insert for the AmpliChip CYP 450 test, lists an incorrect part number for DNase I. The DNase is listed in the "Other Materials Required" section as 'DNase I rec., RNase-free, P/N 04716728001 (Roche Applied Science)" . The Part Number listed for the DNase I listed is incorrect and of lower specific activity than the correct/validated DNase.

FDAMar 9, 2007CA, FL, IN +4 more• Roche Molecular Systems, Inc.

Roche Molecular Systems, Inc.: AmpliChip CYP450 Test-US IVD-M/N: 4591402190, Roche Molec...

FDAMar 9, 2007CA, FL, IN +4 more• Roche Molecular Systems, Inc.