FDAMarch 18, 2016drug

8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL), 4.2 grams (84 mg/mL), 50 mL, Rx only, Hospira Inc, Lake Forest, IL 60045, NDC 0409-6625-02

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

The hazard

Presence of Particulate Matter: particulate matter identified as an insect in one vial.

What to do

FDA enforcement status: Ongoing

Brands named

hospira

Recall history

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

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