FDANovember 12, 2021device

Flexor Check-Flo Introducer Ansel Modification Model Number: KCFW-6.0-18/38-45-RB-ANL0-HC Order Number/GPN: G44154 Intended to introduce therapeutic or diagnostic devices into the vasculature, excluding coronary and neuro vasculature.

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

The hazard

Flexor Check-Flo Introducer Ansel Modification mislabeled. Products packaged with a label stating 6FR may contain a 7FR device and vice versa

What to do

FDA enforcement status: Terminated

Brands named

cook

UPCs

00827002441545

Recall history

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

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Flexor Check-Flo Introducer Ansel Modification Model Number: KCFW-6.0-18/38-45-RB-ANL0-HC Order Number/GPN: G44154 Intended to introduce therapeutic or diagnostic devices into the vasculature, excluding coronary and neuro vasculature. — Recall Details · AllClear