ClearanceBrief
Recall Z-0195-2015 ยท OWB Interventional Fluoroscopic X-Ray System

GE OEC Medical Systems, Inc

Series OEC 9800. The Series OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient,during diagnostic, surgical and interventional procedures.

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
Quantity311
DistributionWorldwide Distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K021049OEC 9800 PLUS DIGITAL MOBILE IMAGING SYSTEM
Ge Oec Medical Systems, Apr 17, 2002
K022069OEC FLUOROTRAK 9800 PLUS
Ge Oec Medical Systems, Sep 17, 2002
K111551OEC(R) 9800, OEC(R) 9800 PLUS
Ge Oec Medical Systems, Inc., Oct 4, 2011
K132027OEC 9800 PLUS
Ge Oec Medical Systems, Inc., May 1, 2014