FDA recall D-0155-2023

Product

Sodium Chloride Ophthalmic Ointment, USP, 5%, Net Wt. 3.5 g (1/8 oz.) per tube, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-622-35

Reason for recall

CGMP Deviations:

Distribution

Nationwide in the USA

Key facts

Status

Ongoing

Initiation date

2022-10-13

Report date

2023-01-25

Voluntary/Mandated

Voluntary: Firm initiated

Location

Gurnee, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0155-2023