FDAOctober 8, 2018drug

0.9% Sodium Chloride Injection, USP Rx Only a) 250 mL NDC 0409-7983-02; b) 150 mL NDC 0409-7983-61; c) 50 mL NDC 0409-7984-36; d) 100 mL NDC 0409-7984-37, 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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