FDAOctober 8, 2018drug

5% Dextrose Injection, USP, Rx Only, a) 25 mL NDC 0409-7923-20; b) 250 mL NDC 0409-7922-02, Hospira, Inc. Lake Forest, IL 60045

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

The hazard

Lack of Assurance of Sterility; bags have the potential to leak

What to do

FDA enforcement status: Terminated

Brands named

icu medicalicu

Recall history

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

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