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FDADecember 22, 2017device

Arrow¿ Pressure Injectable Two-Lumen PICC Kit, Product Number: EU-05052-HPMSB

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

The hazard

Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.

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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