FDAJune 15, 2017drug

Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution 5 mL , a.) Single-dose vial (NDC 0409-6609-02), b.) 25 vial carton (NDC 0409-6609-25), Rx Only, Mfd by Hospira, INC, Lake Forest, IL 60045 USA

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

The hazard

Lack of Sterility Assurance

What to do

FDA enforcement status: Terminated

Brands named

hospira a pfizerhospira

Recall history

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

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