ClearanceBrief
Recall Z-2027-2012 ยท OXO Image-Intensified Fluoroscopic X-Ray System, Mobile

GE OEC Medical Systems, Inc

OEC 8800 Flexiview designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. The OEC 8800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clinical applications may include cholangiography, endoscopic, urologic, orthopedic, neurologic, vascular,

DateJul 18, 2012 (initiated Nov 19, 2007)
StatusTerminated
ReasonPlease be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC recalled imaging devices OEC 9900, OEC 9800, and OEC 8800 as a result of an FDA inspection identifying that the vertical lift column power supply in the mainframe C-arm is defective and subject to early life failure.
Root causeDevice Design
ActionPlease be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE Healthcare sent an"URGENT RECALL NOTICE" dated February 22, 2008 to all affected customers. The letter identifies the product, problem, and actions to be taken by the customers. Contact the firm at 800-874-7378 for questions concerning this recall.
Quantity1349 units
DistributionWorldwide Distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K003837FLEXIVIEW 8800 DIGITAL MOBILE IMAGING SYSTEM
Ge Oec Medical Systems, Mar 12, 2001