Akorn, Inc. recalls Olopatadine HCl Ophthalmic Solution, USP 0.2%, 2.5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, I
Recalled January 25, 2023 · FDA recall D-0149-2023 · Akorn
Hazard
CGMP Deviations: · FDA Class II
Units
173,928 bottles
Sold at
Nationwide in the USA
Description
CGMP Deviations:
Product
Olopatadine HCl Ophthalmic Solution, USP 0.2%, 2.5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-305-12
Manufacturer(s)
Akorn, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →