FDAJanuary 20, 2016device

Flexor Check-Flo Introducer, Catheter introducer, Catalog #: KCFW-6.0-35-70-RB-HFANL0-HC Intended for introduction of balloons, closed and non-tapered end catheters or diagnostic and interventional devices

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

The hazard

Incorrect packaging. Reports of packages labeled as 6.0Fr actually containing 5.0Fr devices.

What to do

FDA enforcement status: Terminated

Brands named

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Recall history

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

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