Akorn, Inc. recalls GONAK Hypromellose Ophthalmic Demulcent Solution, (25 mg) 2.5%, 15 mL per dropper bottle, For Professional Use in Goinos
Recalled January 25, 2023 · FDA recall D-0140-2023 · Akorn
Hazard
CGMP Deviations: · FDA Class II
Units
196,254 bottles
Sold at
Nationwide in the USA
Description
CGMP Deviations:
Product
GONAK Hypromellose Ophthalmic Demulcent Solution, (25 mg) 2.5%, 15 mL per dropper bottle, For Professional Use in Goinoscopic Examinations, Mfd. by: Akorn, INc., Lake Forest, IL 60045. NDC: 17478-064-12
Manufacturer(s)
Akorn, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →