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Terminated

GE CIC Central Station Monitoring Product, Versions 3.x, 4.0.5, 4.0.6

FDA Recall Z-0030-05 · Posted 2004-10-21

Recalling FirmGeneral Electric Medical Systems Information Technology
Recall StatusTerminated
Product CodeDSI
Date Initiated2004-10-11
Date Terminated2006-07-22
Product Quantity11,778

Reason for Recall

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

Distribution Pattern

Distributed nationwide throughout the United States and worldwide.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K032370CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATIONGe Medical Systems Information Technologies · 2003-08-13

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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