Sodium Chloride Ophthalmic Ointment — Class II drug recall D-0155-2023
Ongoing recall by Akorn, Inc., reported 2023-01-25, distributed nationwide. CGMP Deviations:
| Recall number | D-0155-2023 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Akorn, Inc., Gurnee, IL, United States |
| Recall initiated | 2022-10-13 |
| Classified | 2023-01-13 |
| Reported by FDA | 2023-01-25 |
| Distributed | Nationwide (US) |
| Quantity | 524,506 tubes |
| Reason classes | cgmp |
| NDC | 17478-0622-35 |
| Lot numbers | 0F69A, 0G92A, 0G92B, 0J69A, 0K24A, 0K29A, 0M92A, 0M92B, 0M93A, 1B25A, 1C74A, 1C77A, 1E19A |
| Expiration dates | 2023-05-31, 2023-06-30, 2023-08-31, 2023-09-30, 2023-11-30, 2024-01-31, 2024-02-29, 2024-04-30 |
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:
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0155-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.