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GE Healthcare Integrated IT Solutions

GE Healthcare Integrated IT Solutions Recalls

All product recalls associated with GE Healthcare Integrated IT Solutions.

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Recall Summary

Total Recalls

382

Past Year

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 361–380 of 382 recalls

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

The Centricity PACS RA1000 Workstation Software may manifest certain mammography image display problems only if the images were acquired through GE Senographe versions 2000D, DS or Essential.

FDAJan 12, 2007Nationwide• GE Healthcare Integrated IT Solutions

GE Healthcare: Signa MFO/I Magnetic Resonance System, Model Numbers : 2...

Incorrect patient positioning; when moving the patient into the bore may lead to wrist and hand injury.

FDADec 31, 2006AL, AZ, AR +23 more• GE Healthcare

GE Healthcare: GE LightSpeed Pro 16 (100kW/80kW) Models 2357739, 2357739...

Oil may leak onto the port window of the CT tube and may result in image artifacts that could lead to misdiagnosis.

FDADec 21, 2006

1...17 181920

Page 19 of 20Next

AL, AK, AZ +46 more

• GE Healthcare

GE Healthcare: GE LightSpeed VCT Select / LightSpeed Pro32, Model 512609...

Oil may leak onto the port window of the CT tube and may result in image artifacts that could lead to misdiagnosis.

FDADec 21, 2006AL, AK, AZ +46 more• GE Healthcare

GE Healthcare: GE LightSpeed Xtra / GE LightSpeed RT Pro 16, Model 23746...

Oil may leak onto the port window of the CT tube and may result in image artifacts that could lead to misdiagnosis.

FDADec 21, 2006AL, AK, AZ +46 more• GE Healthcare

GE Healthcare: GE Discovery VCT, Volume PET-CT scanner, Model 5124069-3.

Oil may leak onto the port window of the CT tube and may result in image artifacts that could lead to misdiagnosis.

FDADec 21, 2006AL, AK, AZ +46 more• GE Healthcare

GE Healthcare: GE LightSpeed VCT / Light Speed VCT standard configuratio...

Oil may leak onto the port window of the CT tube and may result in image artifacts that could lead to misdiagnosis.

FDADec 21, 2006AL, AK, AZ +46 more• GE Healthcare

GE Healthcare: The LightSpeed RT16 CT Scanner System is indicated for he...

When the manual cradle release feature on the table is used to move a patient out of the gantry, a discrepancy of up to 6mm between the numerical display on the gantry and the actual position of the table could be introduced.

FDADec 8, 2006PR• GE Healthcare

GE Healthcare: The LightSpeed VCT System is intended for head and whole ...

FDADec 8, 2006PR• GE Healthcare

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

Automatic exposure control (AEC) automatically resets allowing another exposure without requiring manual reset as specified in 21 CFR 1020.31 (a)(3)(iv)

FDANov 1, 2006CO, IL, LA +7 more• GE Healthcare

Ge Healthcare: GE ApexPro CH Telemetry System. The ApexPro Telemetry Sy...

When a patient being monitored with ApexPro/Apex Pro CH Telemetry with ST monitoring disabled is in a pre-existing condition of continuous MESSAGE or ADVISORY level alarm preceding a SYSTEM WARNING level alarm, the SYSTEM WARNING audible alarm and flashing yellow border around the patient panel at the CIC (Clinical Information Center) does not occur.

FDAAug 4, 2006PR• Ge Healthcare

Ge Healthcare: ApexPro FH Telemetry System: composed of six major compon...

System Warning Alarm failure: When a patient being monitored is in a pre-existing condition of continuous MESSAGE or ADVISORY level alarm preceding a SYSTEM WARNING level alarm, the SYSTEM WARNING audible alarm and flashing yellow border around the patient panel at the CIC does not occur.

FDAJun 23, 2006Nationwide• Ge Healthcare

GE Healthcare: GE Innova 2100-IQ Digital Fluoroscopic Imaging System, Ve...

The systems do not contain a certification label on the C2 Cabinet (Beam-limiting control).

FDAJun 6, 2006AL, AZ, AR +27 more• GE Healthcare

GE Healthcare: Fresh Gas Control (A-FGC1) Unit, a component of the S/5 A...

There exists the possibility that the ADU Fresh Gas Control unit (A-FGC1) can shut off during normal handling of the anesthesia machine and result in no anesthetic agent output.

FDAMar 22, 2006CA, FL, IL +5 more• GE Healthcare

GE Healthcare: GE Healthcare Innova 3100 and Innova 3100 with Bolus Chas...

Incorrect screws were used for mounting the detector which may lead to a possible part falling onto a patient.

FDAMar 6, 2006Nationwide• GE Healthcare

GE Healthcare: GE Healthcare Innova 4100 and Innova 4100 with Bolus Chas...

Incorrect screws were used for mounting the detector which may lead to a possible part falling onto a patient.

FDAMar 6, 2006Nationwide• GE Healthcare

GE Healthcare: GE Medical Systems Innova 2000 and Innova 2000S, and Inno...

Incorrect screws were used for mounting the detector which may lead to a possible part falling onto a patient.

FDAMar 6, 2006Nationwide• GE Healthcare

GE Healthcare: Datex-Ohmeda S/5 Anesthesia Delivery Unit (ADU)

Alarm sound-It is possible that the audible alarms from the speaker from the Datex-Ohmeda S/5 Anesthesia Delivery Unit (ADU) machine may dampen or disappear as a result of normal handling of the anesthesia machine. Visual alarms on the ADU are unaffected by this condition. The dampening or absence of audible alarms on the ADU may result in a delay in treatment.

FDANov 16, 2005AZ, CA, IA +3 more• GE Healthcare

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

GE Healthcare: GE Millennium Systems: MC, MyoSight. Dual Head Gamma Ca...

In certain cases, one of the four collimator locking mechanisms that attach the collimator to the head may work itself free if collimator exchange has not been performed for an extended period of time. This situation, if neglected, could eventually cause the locking mechanism to unlock itself.

FDAApr 18, 2005Nationwide• GE Healthcare