GE OEC Medical Systems, Inc OEC FluoroTrak 9800 PLUS, image-intensified fluoroscopic x-ray system, GE Healthcare, Salt Lake City, UT. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
OEC FluoroTrak 9800 PLUS, image-intensified fluoroscopic x-ray system, GE Healthcare, Salt Lake City, UT.
Brand
GE OEC Medical Systems, Inc
Lot Codes / Batch Numbers
Serial numbers: 89-1579-N, 89-2529-N, 82-2160-N, 8S-1932-N, 8S-2226-N.
Products Sold
Serial numbers: 89-1579-N, 89-2529-N, 82-2160-N, 8S-1932-N, 8S-2226-N.
GE OEC Medical Systems, Inc is recalling OEC FluoroTrak 9800 PLUS, image-intensified fluoroscopic x-ray system, GE Healthcare, Salt Lake City due to During routine service, primary and/or secondary collimators may not have been properly reinstalled.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
During routine service, primary and/or secondary collimators may not have been properly reinstalled.
Recommended Action
Per FDA guidance
Customers were notified by letter on 03/01/2007. They were told to continue using the machines and that an inspection would be scheduled immediately to verify that collimators had been correctly installed.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026