GE OEC Medical Systems, Inc MiniView 6800 Digital Mobile C-arm fluoroscopic x-ray system. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MiniView 6800 Digital Mobile C-arm fluoroscopic x-ray system.
Brand
GE OEC Medical Systems, Inc
Lot Codes / Batch Numbers
All MiniView 6800 systems.
Products Sold
All MiniView 6800 systems.
GE OEC Medical Systems, Inc is recalling MiniView 6800 Digital Mobile C-arm fluoroscopic x-ray system. due to Radiation exposure rate could exceed specifications during fluoroscopic x-ray procedure.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Radiation exposure rate could exceed specifications during fluoroscopic x-ray procedure.
Recommended Action
Per FDA guidance
Consignees were notified by letter prior to 04/28/2006.
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