D-0135-2023 Class II Ongoing

Recalled by Akorn, Inc. — Gurnee, IL

Recall Details

Product Type
Drugs
Report Date
January 25, 2023
Initiation Date
October 13, 2022
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
6,273 bottles

Product Description

Betaxolol Ophthalmic Solution, USP 0.5%, (Betaxolol HCl 5.6 mg/mL), 5 mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-705-10

Reason for Recall

CGMP Deviations:

Distribution Pattern

Nationwide in the USA

Code Information

Lot: 1A08A, EXP 12/31/2022