FDANovember 27, 2019drug

25% Dextrose Injection, USP 2.5 grams (250 mg/mL) 10 mL Single-dose, Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-1775-10

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

The hazard

Labeling: Incorrect or Missing Lot and/or expiration date.

What to do

FDA enforcement status: Terminated

Brands named

pfizer

Recall history

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

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