US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 21, 2016 (10 years ago)

Sodium Chloride Ophthalmic Solution, USP, 5%, 15 mL (0.5 fL oz.) bottle, Akorn, Inc…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

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

Recalling firm
Akorn Inc
NDC code
17478-623-12
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0124-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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