Drug recall
ImproVue Ophthalmic Lubricant Drops (1.7% Hypromellose), 1 Single Use Syringe, 0.07 fl oz (2mL), 1 Single Use…
FDA recall event 72111 · Class III · Oasis Medical, Inc.
Key facts
| Event ID | 72111 |
|---|---|
| Recall numbers | D-1418-2015 |
| Recalling firm | Oasis Medical, Inc. |
| Product type | Drugs |
| Products | 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… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Falied pH specification |
| Initiation date | Aug 31, 2015 |
| Report date | Sep 16, 2015 |
| Termination date | Dec 18, 2015 |
| City | Glendora |
| State | CA |
| Country | United States |
| FEI number | 2083373 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: