Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions Recalls

All product recalls associated with GE Healthcare Integrated IT Solutions.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

123

Class I (Serious)

Most Recent

Nov 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 2201–2220 of 2383 recalls

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation (for diagnostic ima...

Software anomalies result in patient safety issues involving patient jacket content intermittently becoming unintentionally out of synchronization with the images being displayed, and involving Default Display Protocols (DDPs) which are used to layout images when displaying a study. If the user does not check the Study Date Time of the exam on the image title bar, then they may interpret the curr

FDASep 25, 2008Nationwide• GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions: Centricity Perinatal (formerly Quantitative Sentinel) Sys...

On the I&O chart, the IN, OUT and NET fluid totals values will not honor the numeric precision configuration, always displaying a whole number, losing decimal point accuracy.

FDASep 25, 2008Nationwide• GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions: GE Centricity Ultra Laboratory System Software; for recor...

1...109 110111112 113...120

Page 111 of 120Next

Software computer, error: The abnormal result flag is not being sent in the HL7 messages on results that are lower than the normal range. For further information, please telephone GE Healthcare Integrated IT Solutions at 800-437-1171.

FDASep 22, 2008Nationwide• GE Healthcare Integrated IT Solutions

TomoTherapy Incorporated: TomoTherapy HI-ART Systems with 3.1.2, 3.1.3 or 3.2.1 sof...

TomoTherapy Inc. discovered an issue on the Hi-Art system during the course of ongoing testing. It has been identified that treatment plans involving very small structures (volume <2cc), reading in a high dose gradient region, may exhibit inaccuracies with the DVH curve and the Dose Statistics for the small structures. This error can only happen if planning was performed using very small voxels

FDASep 18, 2008AL, AK, AZ +35 more• TomoTherapy Incorporated

Datex - Ohmeda, Inc: GE Datex-Ohmeda Aisys, Datex-Ohmeda, Inc., a General Ele...

The electronic vaporization system in the GE Aisys Anesthesia machine contains the following components: Backpressure Valve, Inflow Check Valve and Cassette Interface Board, that can contribute to independent failures.

FDAAug 28, 2008AL, AK, CA +27 more• Datex - Ohmeda, Inc

Wooden Infant Toys (Habermaass) – Choking Risk (2008)

Choking Hazard

The puzzles, rattle toys, pacifier holders, and stroller toys are wooden and are described in the chart below. "HABA" is printed on them. Model Description Triolino Puzzle Lady bug puzzle is 7 inches x ½ inch thick LUCY Clutching Toy (rattle) Hearts have mirrors and prisms. The rattle is about 4 inches in diameter. Little Heart Clutching Toy (rattle) Heart has mirror. The rattle is about 3 ½ inches in diameter. Pixie's World (rattle) 2.5" rattle with mushroom, flower, person and house with mirror. Belinda Clutching Toy (rattle) Flower clutching toy has face in the middle. The rattle is about 4 inches in diameter. Miro Clutching Toy (rattle) Rattle center contains blue plastic ball with 10 holes. The rattle is about 3 ½ inches in diameter. Bunny Pacifier Holder Pacifier holder is 8.6 inches long with fabric bunny on the end and wooden star with mirror in the middle. Bear Pacifier Holder Pacifier holder is 8.6 inches long with bear at the end and wooden circle with mirror in the middle. Bonita (rattle) 2.5" bouquet of four shapes on wooden ring. Bella (rattle) 3" diameter with four wooden hearts with two mirrors. Pirate Joe (rattle) 4" pirate theme with bell and mirror. Rally (rattle) 4" triangle shape with three cars. Flori (rattle) Six petal shapes on elastic band. Includes three mirrors & three bells. 5" Triola (rattle) 4" triangle with two flowers and round corner. Trio (rattle) 4" triangle shape with squeaker, bell and mirror. Speedy (rattle) Wooden car about 4.5" L x 3" H. Squeaker in back and mirror on car hood. Little Hearts Stroller Toy 18" pram-chain with ten various size wooden hearts. Discovery Balls, Set of 4 Set contains 1 orange, 1 red, 1 blue and one bicolor blue/yellow ball. Red ball contains three small mirrors. Discovery Ball with Rattle Blue/Yellow round wooden ball with small mirror.

CPSCAug 28, 2008Nationwide• Habermaass Corp. Inc., of Skaneateles, N.Y.

Wolf SL Carbon Bicycle Forks (True Temper) – Fall Hazard (2008)

The recalled forks have a clear coating over black painted carbon fiber, with the words "Wolf Superlite" and related logo just below the crown on each fork leg, and the letters "SL" on each leg above the fork blade dropouts. There is a True Temper CRT™ logo on the inside of both fork legs. The recalled forks could have been included on the following bicycle models: R3, R3 SL, Soloist Carbon, Soloist Carbon SL, and certain P3 Carbon framesets and complete bicycles.

CPSCAug 20, 2008Nationwide• True Temper Composite Material Products Co. Ltd, of Guangzhou, China

Vance Products Incorporated: Cook Urological Endoureterotomy Stent Set, 10Fr/13 cm, 6....

The bond may break where the two materials meet, resulting in separation of the stent.

FDAJul 31, 2008Nationwide• Vance Products Incorporated

Reebok Studio Exercise Cycles – Laceration Risk (2008)

Laceration Risk

The Reebok Studio Cycle is an upright exercise bike used primarily in fitness centers and other institutional settings. The recalled bicycle is black with silver cranks. The unit has an internal belt drive. The base of the bicycle is a single piece that is welded to the frame. The legs are two straight horizontal bars with rounded edges. There is a logo located on the side of the exercise cycle that shows a person riding a bicycle.

CPSCJul 24, 2008Nationwide• Fitness Associates Incorporated (F.A.I.), under license from Reebok International Ltd., of Canton, Mass. Note: F.A.I. is no longer in business.

Spacelabs Healthcare, Incorporated: Ultraview SL Command Module, Model 90496 The product is i...

Potential for module to fail to obtain a NIBP reading on hypertension patients.

FDAJul 22, 2008Nationwide• Spacelabs Healthcare, Incorporated

Spacelabs Healthcare, Incorporated: Ultraview Digital Telemetry Transmitter, Model 90478 The ...

Telemetry Modules are failing to alarm for low heart rate and asystole.

FDAJul 18, 2008Nationwide• Spacelabs Healthcare, Incorporated

Spacelabs Healthcare, Incorporated: Ultraview Digital Telemetry Transmitter, Model 91341-09 T...

During battery insertion there is potential for patient waveforms to move to an open receiver module or to an occupied receiver causing the intermittent inappropriate monitoring of both patients for several minutes.

FDAJul 17, 2008Nationwide• Spacelabs Healthcare, Incorporated

Spacelabs Healthcare, Incorporated: Spacelabs Medical Temperature Probe Adaptor PN-700-0031-0...

Intermittent contact of temperature probe adaptors can cause a loss of temperature monitoring which can cause a delay in care when an alarm is missed.

FDAJul 2, 2008Nationwide• Spacelabs Healthcare, Incorporated

GE Healthcare Integrated IT Solutions: GE Healthcare Centricity Perinatal (formerly QS) System -...

Patient information mix-up: When the PFILS application, configured with a backup server has experienced a network interruption, PFILS verify could result in the Centricity Perinatal application recording non-identifiable patient information to the incorrect patient file.

FDAJun 30, 2008PR• GE Healthcare Integrated IT Solutions

Acrymed Incorporated: ON-Q Silver Dressing is a Antimicrobial wound dressing co...

The Silver Dressing, lot H0705J and H0706J may contain dressings that are not properly sealed in the foil pouch, which could affect sterility of the dressing.

FDAJun 30, 2008Nationwide• Acrymed Incorporated

Datex Ohmeda, Inc. dba GE Healthcare: Giraffe OmniBed, labeled in part: ***GE Healthcare 8880...

Manufacturer of neonatal incubators changed the device labeling to account for new use and care instructions.

FDAJun 20, 2008Nationwide• Datex Ohmeda, Inc. dba GE Healthcare

Infra-Red Sauna Rooms (Waterstar Electronic) – fire hazard (2008)

Fire/Burn Risk

The recalled infra-red sauna rooms are made of wood and include the following model numbers: IC I, IC II, IC III, IC IV, and IC V. The model number is indicated on the serial plate located on the back of the machine, in the lower right hand corner. IC I (1-Person) Dimensions: 35.5"x41.5"x75"(in) IC II (2-Person) Dimensions: 47"x47"x75"(in) IC III (3-Person) Dimensions: 60"x49"x75"(in) IC IV (4-Person) Dimensions: 69"x53"x75"(in) IC V (Corner) Dimensions: 59"x23.5"x49x75"(in)

CPSCJun 12, 2008Nationwide• Xuzhou Waterstar Electronic Co.

GE Healthcare Integrated IT Solutions: GE Centricity AW Suite software version 2.0 and 2.0.1 wit...

When using any vessel analysis protocol of the AW Suite Card IQ application, the software can reload saved tracking objects (Save State) incorrectly and display an incorrect vessel label over the restored images. This failure only occurs when users create a custom label in the vessel analysis protocol and include leading or trailing blank characters (space bar) in the custom label.

FDAJun 11, 2008Nationwide• GE Healthcare Integrated IT Solutions

VISX INCORPORATED, A SUBSIDIARY OF AMO INC: AMO WaveScan WaveFront System Version 3.90/3.901, Part Nu...

Inaccurate measurements may be generated by the device, which could result in improper treatment and deterioration of patient eyesight.

FDAJun 9, 2008Nationwide• VISX INCORPORATED, A SUBSIDIARY OF AMO INC

Datex Ohmeda, Inc. dba GE Healthcare: Panda iRes and Giraffe Infant Warmers, labeled in part***...

Medical device software may be subject to signal interference of the Hands Free Alarm Silence feature that could impact patient safety.

FDAMay 20, 2008Nationwide• Datex Ohmeda, Inc. dba GE Healthcare