RecallRadar

FDA Drug recall D-0157-2023

Tobramycin Ophthalmic Solution, USP, 0.3%, 5 mL per dropper bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045

On 2023-01-25 the FDA classified a Class II recall of Tobramycin Ophthalmic Solution, USP, 0.3%, 5 mL per dropper bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045 by Akorn, citing CGMP Deviations:.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0157-2023
ClassificationClass II
Statusongoing
Initiated2022-10-13
Published2023-01-25
Last updated2026-09-13 11:52 UTC
CompanyAkorn
DistributionUS

Product

Tobramycin Ophthalmic Solution, USP, 0.3%, 5 mL per dropper bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC 17478-290-10

Reason

CGMP Deviations:

Identifiers

code_infoLot: 1C56A, EXP 2/28/2023; 1J50A, EXP 8/31/2023; 1K61A, EXP 9/30/2023 ; 1M27A, EXP 11/30/2023;

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0157-2023%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.