FDADecember 22, 2017device

Multi-Lumen Hemodialysis Catheterization Kit for High Volume Infusions, Part Number: CDC-12123-P1A

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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