ClearanceBrief
Recall Z-0975-2017 ยท OXO Image-Intensified Fluoroscopic X-Ray System, Mobile

GE OEC Medical Systems, Inc

The OEC 9900 Elite mobile fluoroscopy system is designed to provide fluoroscopic and spot-film images of the patient during diagnostic surgical and interventional procedure. Examples of clinical application may include cholangiography, endoscopy, urologic, orthopedic, neurologic, vascular, cardiac, critical care and emergency room procedure. The system may be used for other imaging applications at

DateJan 9, 2017 (initiated Dec 19, 2016)
StatusTerminated
ReasonGE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.
Root causeUse error
ActionGE Healthcare sent an Urgent Medical Device Correction letter dated December 19, 2016, to all affected consignees. GE informed consignees that GE will correct all affected products. If consignnes have any questions or concerns regarding this notification, please contact GE Healthcare Service at 1-800-437-1171 or their local Service Representative. For questions regarding this recall call 801-536-4952.
DistributionWorldwide Distribution - US including U.S. States: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PUERTO RICO, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and Internationally to Canada, Mexico, an
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K120613OEC 9900 ELITE
Ge Healthcare Surgery GE Oec Medical Systems, Inc., Apr 6, 2012
K122234OEC 9900 ELITE
Ge Healthcare Surgery GE Oec Medical Systems, Inc., Aug 16, 2012