FDAJuly 27, 2017device

Empty IntraVia Container with Non-DEHP Fluid Path, 500mL Containers are intended for use in the preparation and administration of drug admixtures.

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

The hazard

A leak may allow for microbial contamination of the sterile fluid path.

What to do

FDA enforcement status: Terminated

Brands named

baxter healthcarebaxter

Recall history

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

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