FDAOctober 21, 2016drug

Sodium Chloride Ophthalmic Solution, USP, 5%, 15 mL (0.5 fL oz.) bottle, Akorn, Inc., Lake Forest, IL 60045, NDC 17478-623-12.

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

The hazard

Subpotent Drug: concentration of product is less than labeled amount.

What to do

FDA enforcement status: Terminated

Brands named

akorn

Recall history

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

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