FDAMarch 31, 2017device

Endopath ETS-FLEX Endoscopic Articulating Linear Cutter, VASCULAR/THIN 35MM

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

The hazard

There is a risk that the pinion gear in the device could fail under extreme use cases.

What to do

FDA enforcement status: Terminated

Brands named

ethicon endo surgeryethiconethicon endo

Recall history

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

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