Medical Device Recall: Z-0030-05

FDA Recalls dataset · Firm: General Electric Medical Systems Information Technology · Status: Terminated

Recall Action Class: N/A Date Initiated: 2004-10-11 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0030-05.

Recall Res Number
Z-0030-05
FEI Number
2124823
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2004-10-11
Date Posted
2004-10-21
Date Terminated
2006-07-22
Product Code
DSI
Event Number
30018
Product Quantity
11,778
Product Description GE CIC Central Station Monitoring Product, Versions 3.x, 4.0.5, 4.0.6
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.
Action Details N/A
Distribution Pattern Distributed nationwide throughout the United States and worldwide.
Code Information / Serial Numbers All serial numbers for versions 3.x, 4.0.5, and 4.0.6

Related Establishments / Registrations

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