GE OEC Medical Systems, Inc OEC Uroview 2800 with Dual Monitor Option, fluoroscopic x-ray system, Model Numbers: 882082-01, 882082-02, 886765-01, GE Healthcare, Surgery, Salt Lake City, UT. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
OEC Uroview 2800 with Dual Monitor Option, fluoroscopic x-ray system, Model Numbers: 882082-01, 882082-02, 886765-01, GE Healthcare, Surgery, Salt Lake City, UT.
Brand
GE OEC Medical Systems, Inc
Lot Codes / Batch Numbers
Model Numbers: 882082-01, 882082-02, 886765-01. Units with manufactured dates between 03/2003 and 08/2006.
Products Sold
Model Numbers: 882082-01, 882082-02, 886765-01. Units with manufactured dates between 03/2003 and 08/2006.
GE OEC Medical Systems, Inc is recalling OEC Uroview 2800 with Dual Monitor Option, fluoroscopic x-ray system, Model Numbers: 882082-01, 8820 due to Uroview 2800 system with dual monitors may pose a safety risk to patients if the monitors become disconnected and fall.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Uroview 2800 system with dual monitors may pose a safety risk to patients if the monitors become disconnected and fall.
Recommended Action
Per FDA guidance
Consignees were notified by letter on 01/15/2007. Instructions were given to position and not move the dual monitors until inspection and correction by GE personnel. For the affected units with a 3 phase power distribution box, users were cautioned to ensure that the access door to the power box is completely closed when the unit is powered on to prevent a shock hazard.
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