FDAJune 15, 2017drug

8.4% Sodium Bicarbonate Inj., USP 50 mL Single-dose, 50 mEq (1 mEq/mL) 4.2 grams (84 mg/mL), Rx Only, Mfd by Hospira, INC, Lake Forest, IL 60045 USA, NDC: 0409-6625-02

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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