FDA Drug recall D-1084-2015
ImproVue Ophthalmic Lubricant Drops (1.7% Hypromellose), 1 Single Use Syringe, 0.07 fl oz (2mL), 1 Single Use Applicator Tip per carton, Ma…
- FDA Drug
- Class III
- terminated
- Published 2015-05-27
On 2015-05-27 the FDA classified a Class III recall of ImproVue Ophthalmic Lubricant Drops (1.7% Hypromellose), 1 Single Use Syringe, 0.07 fl oz (2mL), 1 Single Use Applicator Tip per carton, Ma… by Oasis Medical, citing failed pH specification.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1084-2015 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2015-04-10 |
| Published | 2015-05-27 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Oasis Medical |
| Distribution | FL |
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
Failed pH specification
Identifiers
| code_info | Lot# V0814B, Exp 02/16; V1014H, Exp 04/16 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1084-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.