FDAOctober 5, 2016device

OSCOR ADELANTE BREEZEWAY 8F C120¿ S79CM D84CM Catalog # AB081047 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.

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

The hazard

Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.

What to do

FDA enforcement status: Terminated

Brands named

oscor

Recall history

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

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