General Electric Medical Systems Information Technology GE CIC Central Station Monitoring Product, Versions 3.x, 4.0.5, 4.0.6 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
GE CIC Central Station Monitoring Product, Versions 3.x, 4.0.5, 4.0.6
Brand
General Electric Medical Systems Information Technology
Lot Codes / Batch Numbers
All serial numbers for versions 3.x, 4.0.5, and 4.0.6
Products Sold
All serial numbers for versions 3.x, 4.0.5, and 4.0.6
General Electric Medical Systems Information Technology is recalling GE CIC Central Station Monitoring Product, Versions 3.x, 4.0.5, 4.0.6 due to The following two conditions may occur with the printing of full disclosure strips and reports, printing of the alarm history events stored on a GE U. Based on FDA medical device recall database.
Summary derived from FDA notice
The following details were not provided by the FDA: corrective action details.
Reason for Recall
As stated by FDA
The following two conditions may occur with the printing of full disclosure strips and reports, printing of the alarm history events stored on a GE Unity Network Patient Data Server (PDS), and printing of caliper reports in the GE CIC Pro central station monitoring product, 1) a delay or cessation in updating portions of th display screen: or, 2) System reset/restart.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026