FDAJune 12, 2017device

Arrow Glide Thru Peel-Away Sheath/Dilator Introducer

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

The hazard

Arrow is recalling additional lots that were identified as part of an active recall. Arrow is recalling the affected product due to the possibility that the catheter peel-away component hub tabs may prematurely detach when the practitioner begins to peel apart the sheath body from the catheter.

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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