FDAJuly 21, 2022device

Medline CHEST TUBE REORDER NO: DYNJ36762A

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

The hazard

Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit

What to do

FDA enforcement status: Ongoing

Brands named

medline

UPCs

101934898944040193489894401

Recall history

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

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