Events

Recall of CIC Pro Clinical Inforamtion Center Central Information Central Station

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by General Electric Medical Systems Information Technology.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    30018
  • Event Risk Class
    Class 2
  • Event Number
    Z-0030-05
  • Event Initiated Date
    2004-10-11
  • Event Date Posted
    2004-10-21
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2006-07-22
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=35018
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Detector And Alarm, Arrhythmia - Product Code DSI
  • 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.

Device

CIC Pro Clinical Inforamtion Center Central Information Central Station

Manufacturer

General Electric Medical Systems Information Technology
  • Manufacturer Address
    General Electric Medical Systems Information Technology, 8200 W Tower Ave, Milwaukee WI 53223-3219
  • Source
    USFDA