ClearanceBrief
Recall Z-0193-2015 ยท OXO Image-Intensified Fluoroscopic X-Ray System, Mobile

GE OEC Medical Systems, Inc

OEC MiniView 6800. The Mini 6800 Digital Mobile C-Arm is designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imaging. The device is not intended for whole-body pediatric imaging.

DateNov 7, 2014 (initiated Oct 3, 2014)
StatusTerminated
ReasonGE Healthcare initiated a field correction because prior revision of components were potentially installed on certain OEC 9800, FlexiView 8800, OEC MiniView 6800 and OEC UroView 2800 systems.
Root causeComponent design/selection
ActionOn October 3. 2014. GE Healthcare Surgery began distributing an Urgent Medical Device Correction letter to customers 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: 1.1 Facility Administrator. 2.1 Director/Manager of Radiology and Radiologists, 3.) Radiology Department. Firm will track all service requests for the field action to completion. These service requests will document the inspection and component replacement (if applicable) on the affected units. Exceptions to completion of the serv
Quantity26
DistributionWorldwide Distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K992506MINI 6800 DIGITAL MOBILE C-ARM
Ge Dec Medical Systems, Aug 19, 1999