Moisturizing Lubricant Eye Drops — Class II drug recall D-0511-2019
Terminated recall by Akorn Inc, reported 2019-02-27, distributed nationwide. Failed Stability Specification: out of specification results for Sodium Perborate
| Recall number | D-0511-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Recalling firm | Akorn Inc, Lake Forest, IL, United States |
| Recall initiated | 2019-02-04 |
| Classified | 2019-02-19 |
| Reported by FDA | 2019-02-27 |
| Terminated | 2022-07-29 |
| Distributed | Nationwide (US) |
| Quantity | 78,120 dropper |
| Reason classes | specification failure |
| NDC | 00363-9651-01 |
| Lot numbers | 03/20, 07/19, 10/19, 7H98A, 7L80A, 8D31A |
Product
Moisturizing Lubricant Eye Drops, 0.25% Sodium Carboxymethylcellulose, 0.5 Fl OZ (15mL) Distributed by: Walgreen Co, 200 Wilmont Rd Deerfield IL 60015 NDC 00363-9651-01.
Reason for recall
Failed Stability Specification: out of specification results for Sodium Perborate
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-0511-2019. 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.