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FDAJanuary 10, 2019device

Arrow¿ Two-Lumen Central Venous Catheterization Set with Blue FlexTip¿ Catheter Product Code: CD-10802 GTN: 00801902015396

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

The hazard

The product lidstock contains a labelling error. The lidstock states the incorrect priming volume. The priming volumes printed on the extension lines are correct

What to do

FDA enforcement status: Terminated

Brands named

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UPCs

00801902015396

Recall history

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

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