FDADecember 19, 2016device

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...

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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