FDA Medical Device Recalls (openFDA)
General Electric Medical Systems Information Technology: GE CIC Central Station Monitoring Product, Versions 3.x, 4.0.5, 4.0.6
- Recall number
- Z-0030-05
- Recalling firm
- General Electric Medical Systems Information Technology
- Product
- GE CIC Central Station Monitoring Product, Versions 3.x, 4.0.5, 4.0.6
- Status
- Terminated
- Initiated
- 2004-10-11
- Posted
- 2004-10-21
- Terminated
- 2006-07-22
- Reason
- 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.
- Root cause
- Other
- Action
- not on file
- Quantity
- 11,778
- Distribution
- Distributed nationwide throughout the United States and worldwide.
- Lot, serial or model codes
- All serial numbers for versions 3.x, 4.0.5, and 4.0.6
- 510(k) numbers
- ["K032370"]
- PMA numbers
- not on file
- Product code
- DSI
- Firm FEI
- 2124823
- Firm city
- Milwaukee
- Firm state
- WI
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28