GE OEC Medical Systems, Inc: Medical Device Recalls in 2017

According to to data from the FDA, there were 6 medical device recalls made by GE OEC Medical Systems, Inc in 2017. See the details of the recalls below.

You can see similar recalls for other firms.

• 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 the physician's discretionOEC 9900 Elite. MDL Numbers: D148942, D155043
• OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clinical application may include cholangiography, endoscopy, urologic, orthopedic, neurologic, vascular, cardiac, critical care and emergency room procedures.
• OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 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
• OEC 9800. MDL Numbers: D222250, D141598
• OEC 9900 Elite. MDL Numbers: D148942, D155043
• OEC FlexiView 8800, Digital Mobile Imaging System, GE Medical Systems