FDA Recall Terminated

NX 2008 Central Monitoring System (CMS). Product code: E2FB6 Agfa's Computed Radiography Systems with NX Workstations are intended for use in providing diagnostic quality images to aid the physician with diagnosis.

Recall: Z-1889-2009 · Initiated June 22, 2009

Recall

Recall Number
Z-1889-2009
Event Number
52679
Firm
AGFA Corp.
FEI Number
3001236302
Product Code
LLZ
Status
Terminated
Root Cause
Software design
Initiated
June 22, 2009
Posted
September 2, 2009
Terminated
July 22, 2010
Address
10 S Academy St, Greenville, SC, 29601-2632

Description

NX 2008 Central Monitoring System (CMS). Product code: E2FB6 Agfa's Computed Radiography Systems with NX Workstations are intended for use in providing diagnostic quality images to aid the physician with diagnosis.

Reason

After opening and closing a study on a Central Monitoring System while a study is still open on an in-room NX system, a problem of image mix-up can occur on the in-room NX system.

Action

An "Urgent Safety Notice" was sent to all potentially affected sites on/about June 22, 2009 to make them aware of the issue. A FAX Back form is requested with each letter to ensure someone at the account acknowledges the information was received and understood. If a FAX Back form is not received, the account will be contacted by telephone. A software service update to solve this issue is expected to be released by August 15, 2009. A Mandatory Service Bulletin will be deployed to correct the problem in the software. If you have questions, please contact Agfa Healthcare at 1-800-581-2432 prompts 1, 3 and then 2 for CR Support.

Distribution

Worldwide - IL, PA, TX, Canada, Europe, Asia Pacific and Latin America

Quantity

97 units