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Datex Ohmeda, Inc. dba GE Healthcare

Datex Ohmeda, Inc. dba GE Healthcare Recalls

All product recalls associated with Datex Ohmeda, Inc. dba GE Healthcare.

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Recall Summary

Total Recalls

1000

Past Year

593

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 9461–9480 of 10391 recalls

Datex Ohmeda, Inc. dba GE Healthcare: Corometrics MODEL 250 Series Maternal/ Fetal Monitor, Mod...

Communication connector within monitor is defective and may cause potential loss of telemetry.

FDAMay 5, 2008Nationwide• Datex Ohmeda, Inc. dba GE Healthcare

GE Healthcare: GE Precision RXi Digital remote X-Ray Imaging R&F System,...

The Precision RXi collimator did not contain a label identifying the device as being certified to comply with applicable requirements of the x-ray performance standard.

FDAMay 1, 2008AK, CO, IL +15 more• GE Healthcare

GE Healthcare: GE Precision MPi, model 2385125. GE Medical Systems - Am...

The Precision MPi collimator did not contain a label identifying the device as being certified to comply with applicable requirements of the x-ray performance standard.

FDA

1...472 473474475 476...520

Page 474 of 520Next

May 1, 2008

CA, CO, FL +11 more

• GE Healthcare

ThermoFisher Scientific Co., LLC: 10% Buffered Formalin Phosphate; Certified For laboratory...

Assay tests on retention sample of 10% Buffered Formalin Phosphate showed it to be 3.417%, which is below the specification of 4-5%.

FDAMay 1, 2008Nationwide• ThermoFisher Scientific Co., LLC

GE Healthcare: Advantage Workstation version 4.2P, 4.3 and 4.4 with Volu...

GE Healthcare has recently became aware of a possible mismatch between the label of the tracked vessel and the underlying image associated with the cardio- vascular applications of the Advantage workstation that may impact patient safety.

FDAMay 1, 2008AL, AK, AZ +47 more• GE Healthcare

GE Healthcare: GE Precision MPi, model 5126893. GE Medical Systems - Am...

The Precision MPi collimator did not contain a label identifying the device as being certified to comply with applicable requirements of the x-ray performance standard.

FDAMay 1, 2008CA, CO, FL +11 more• GE Healthcare

GE Healthcare: GE Precision MPi, model 2398238. GE Medical Systems - Am...

The Precision MPi collimator did not contain a label identifying the device as being certified to comply with applicable requirements of the x-ray performance standard.

FDAMay 1, 2008CA, CO, FL +11 more• GE Healthcare

Rio Beach High-Boy Chairs – Fall Hazard (2008)

This recall involves the Rio Beach® High-Boy folding beach chairs with UPC and model numbers listed below. The chairs have aluminum tubing frames, striped or solid color fabric slings, and wood arms with an attached storage pouch with cell phone pocket. "Rio Beach® High-Boy", the UPC number and the model number can be found on the hand tag and on a sticker on the rear leg. MODEL # UPC # SC640-702 0-80958-26396-2 SC640-812 0-80958-26465-5 SC640-818 0-80958-26466-2 SC640-8182 0-80958-27165-3 SC641-084-BB 0-80958-27015-1

CPSCApr 29, 2008Nationwide• Rio Brands, of Philadelphia, Pa.

DePuy Mitek, Inc., a Johnson & Johnson Co.: Lupine BR Anchor w/Orthocord TCP/PLGA Absorbable Anchor, ...

Lupine BR Anchor w/Orthocord was assembled with an incorrect suture configuration. The suture loop was not assembled at the distal end of the anchor. It was only threaded through the suture hole in the anchor. Risk associated with incorrect suture configuration include premature breakage.

FDAApr 29, 2008CA, MD, MA +5 more• DePuy Mitek, Inc., a Johnson & Johnson Co.

Siemens Healthcare Diagnostics, Inc.: Siemens Stratus CS Acute Care Troponin I CalPak. In vitr...

The firm received and confirmed that some lots of Cardiac Troponin I (cTnl) CalPaks (CCTNI-CR) may exhibit calibration issues that cause lower than typical signal during calibration with the current population of cTnl TestPaks (CCTNI). This issue may result in failed calibrations due to "Slope Error" messages or falsely elevated patient sample and quality control (QC) results on calibrations that

FDAApr 28, 2008Nationwide• Siemens Healthcare Diagnostics, Inc.

GE Healthcare: GE Datex-Ohmeda Engstrom Carestation The Carestation cons...

There is a correction associated with Engstrom Carestation with an integrated Aerogen Professional Nebulizer System. There is an issue relating to the removal of the nebulizer cable from nebulizer connection port, which, when done while the nebulizer is active, may result in the discontinuance of mechanical ventilation. This issue affects all of the Engstrm Carestations shipped between 12/4/2006

FDAApr 23, 2008GA, IN, NM +5 more• GE Healthcare

Smith & Nephew Inc: TRIGEN Hind Foot Fusion Nail, 10mm X 25mm Left, REF 71701...

One of the distal locking screw holes on a hindfoot fusion nail was drilled with an incorrect trajectory.

FDAApr 22, 2008Nationwide• Smith & Nephew Inc

Siemens Healthcare Diagnostics, Inc.: Dimension Flex Reagent Cartridge C-Reactive Protein Exten...

falsely elevated results in EDTA plasma samples

FDAApr 15, 2008Nationwide• Siemens Healthcare Diagnostics, Inc.

Lithium-Polymer Battery Chargers (Art-Tech) – Fire Risk (2008)

Fire/Burn Risk

The recall involves a lithium-polymer battery charger and batteries sold with the AT600 Falcon Helicopter kit. The recall also includes any spare battery (Model AT600B) or spare charger (Model ATS6046) purchased for this kit.

CPSCApr 14, 2008Nationwide• Art-Tech R/C Hobby Co., Ltd. of Shenzhen, China

Philips Medical Systems North America Co. Phillips: NeuViz Dual Multi-Slice Computed Tomography (CT) Scanner ...

An issue associated with the "Timed Scan" application was found. The system does not wait for the programmed time interval and starts the x-ray after selection of the scan button when certain criteria is met.

FDAApr 10, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Essenta DR - digital multifunctional x-ray system (applic...

Bright artifacts may appear on a patient image from a previous exposure, which might lead to a misdiagnosis.

FDAApr 8, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Siemens Healthcare Diagnostics, Inc.: Dimension Cardiac Troponin I Flex reagent cartridge (CTN...

possibility of falsely elevated results

FDAApr 8, 2008Nationwide• Siemens Healthcare Diagnostics, Inc.

Gas Water Heaters (A.O. Smith) – Fire Hazard (2008)

Fire/Burn Risk

This recall involves 75-gallon natural and propane gas water heaters. "A.O. Smith" or "State" is printed on the side of the unit. A.O. Smith and State model and serial numbers included in this recall are listed in the chart below. Model and serial numbers are printed on the water heater's rating plate. Brand Name Model Number A.O. Smith FCG-75 300 Serial Number Ranges L07A071460 through L07A144966 or M07A009387 through M07A072884 FCG-75 301 State GS6 75 XRR S GS6 75 CRR S

CPSCApr 3, 2008Nationwide• A.O. Smith Water Products Co., of Ashland City, Tenn.

Imaginarium Activity Centers – Choking Hazard (2008)

Choking Hazard

This recall involves the Imaginarium Multi-Sided and Jungle activity centers. The multi-sided activity center has moveable block letters, clock face, sliding shapes and gears. The jungle activity centers have peg jumping monkeys, sliding fish, abacus beads, bead mazes and other animal-themed activities. "Imaginarium" and the name of the activity center are printed on the packaging. Item numbers 69042 (multi-sided) and 69083 (jungle) are printed on the back of the box, near the bar code.

CPSCApr 3, 2008Nationwide• Taizhou Orient Toys Company Ltd. (Multi-Sided Activity Centers), of Shanghai, China

GE Healthcare: GE Healthcare Solar 8000M System, a multiparameter physio...

A software error has been discovered when using Combination Monitoring with Solar 8000M/i - PDM - Telemetry in combo mode. This error has only been noted with this particular configuration and mode of monitoring. It has not been observed in other monitoring applications. The software error will result in a reset of the Solar 8000M/i, causing a loss of monitoring for approximately 1-2 minutes a

FDAApr 2, 2008Nationwide• GE Healthcare