Refresh Relieva PF Preservative-Free Lubricant Eye Drops 0 — Class II drug recall D-0233-2021
Terminated recall by Allergan, PLC., reported 2021-01-27, distributed nationwide. Labeling: Missing instructions for use insert
| Recall number | D-0233-2021 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Allergan, PLC., Madison, NJ, United States |
| Recall initiated | 2020-12-30 |
| Classified | 2021-01-19 |
| Reported by FDA | 2021-01-27 |
| Terminated | 2023-06-21 |
| Distributed | Nationwide (US) |
| Quantity | 100,634 bottles |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00300236634100 |
| NDC | 00023-6634, 00023-6634-01, 00023-6634-10, 00023-6634-20 |
| Lot numbers | T0392, T0843 |
| Expiration dates | 2022-07-20, 2022-08-20 |
Product
Refresh Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz (10 mL) Sterile Distributed by: Allergan, an AbbVie company Madison, NJ 07940 UPC 3 00236 63410 0, NDC 0023-6634-10.
Reason for recall
Labeling: Missing instructions for use insert
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-0233-2021. 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.