OEC Medical Systems, Inc GE Healthcare OEC 9900 mobile fluoroscopic x-ray system Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
GE Healthcare OEC 9900 mobile fluoroscopic x-ray system
Brand
OEC Medical Systems, Inc
Lot Codes / Batch Numbers
All codes
Products Sold
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OEC Medical Systems, Inc is recalling GE Healthcare OEC 9900 mobile fluoroscopic x-ray system due to Possible overexposure: Failure to apply the entrance exposure rate (EER) tube current limit calibration to the automatic exposure rate (AER) control s. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Possible overexposure: Failure to apply the entrance exposure rate (EER) tube current limit calibration to the automatic exposure rate (AER) control system when the anatomical profile mode is changed from the default selection to another selection. Manual technique modes are not affected.
Recommended Action
Per FDA guidance
GE OEC sent a letter to customers December 15, 2007, and scheduled field representative visits for corrective software solution installation.
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