ClearanceBrief
Recall Z-2628-2016 ยท OWB Interventional Fluoroscopic X-Ray System

GE OEC Medical Systems, Inc

OEC UroView 2800, fluoroscopic x-ray system

DateJul 22, 2016
StatusTerminated
ReasonA firmware issue in the supplied LCD workstation monitor(s). Under some circumstances, the monitor(s) may appear dark with no video displayed.
Root causeSoftware design (manufacturing process)
ActionOn July 22, 2016 GE Healthcare Surgery began distributing an Urgent Medical Device Correction letter to customers via mail to inform them of the issue and provide instructions for immediate mitigation of the issue. The letter was sent to 3 titles at each facility affected: 1.) Facility Administrator, 2.) Director/Manager of Radiology and Radiologists, 3.) Radiology Department. Consignees instructured that local GE Healthcare Field Engineer will contact them to coordinate replacement of the affected monitor(s), and will ensure that system meets specifications.
Quantity47 total
DistributionDistribution US nationwide and Korea.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K993687UROVIEW 2800
Ge Dec Medical Systems, Dec 21, 1999