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FDAMay 9, 2017device

Arrow MAC Two-Lumen Central Venous Access Kit Introducer Catheter The Arrow Two-Lumen Central Venous Access device permits venous access and catheter introduction to the central circulation

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

The hazard

Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.

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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