ImproVue Ophthalmic Lubricant Drops — Class III drug recall D-1084-2015
Terminated recall by Oasis Medical, Inc., reported 2015-05-27, distributed in FL. Failed pH specification
| Recall number | D-1084-2015 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Oasis Medical, Inc., Glendora, CA, United States |
| Recall initiated | 2015-04-10 |
| Classified | 2015-05-21 |
| Reported by FDA | 2015-05-27 |
| Terminated | 2015-12-18 |
| Distributed | FL |
| Quantity | 9,731 cartons |
| NDC | 62144-5510-05 |
| Lot numbers | 02/16, 04/16, V0814B, V1014H |
Product
ImproVue Ophthalmic Lubricant Drops (1.7% Hypromellose), 1 Single Use Syringe, 0.07 fl oz (2mL), 1 Single Use Applicator Tip per carton, Manufactured for OCULUS SURGICAL, Port St. Lucie, FL 34986, NDC 62144-5510-05
Reason for recall
Failed pH specification
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-1084-2015. 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.