FDAJune 23, 2016drug

Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32

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

The hazard

Crystallization: Product contains particulate identified to be crystallized active ingredient.

What to do

FDA enforcement status: Terminated

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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