FDADecember 19, 2016device

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...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

GE 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.

What to do

FDA enforcement status: Terminated

Brands named

ge oec medical systems

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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