Akorn, Inc. recalls Olopatadine HCl Ophthalmic Solution, USP 0.1%, 5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL
Recalled January 25, 2023 · FDA recall D-0151-2023 · Akorn
Hazard
CGMP Deviations: · FDA Class II
Units
121,176 bottles
Sold at
Nationwide in the USA
Description
CGMP Deviations:
Product
Olopatadine HCl Ophthalmic Solution, USP 0.1%, 5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC: 60429-957-05
Manufacturer(s)
Akorn, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →