FDADecember 28, 2017device

NEO-KATH(TM) Caudal Set, REF 201-2430, Sterile

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

The hazard

Potential for stylet to protrude from the distal end of the catheter

What to do

FDA enforcement status: Completed

Brands named

epimed

Recall history

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

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