FDAJune 20, 2018device

The Tri-Flo Subglottic Suction System

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

The hazard

Vyaire Medical has discovered potential patient safety risk with associated with the Tri-Flow Subglottic Suction System. The distal soft tip of the catheter has been identified as having the potential to break off during patient use and result in aspiration of a solid foreign body.

What to do

FDA enforcement status: Terminated

Brands named

vyaire medicalvyaire

Recall history

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

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