# FDA recall D-1084-2015

> **Oasis Medical, Inc.** · Class III · drug recall initiated 2015-04-10.

## 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

## Distribution

FL

## Key facts

- **Recall number:** D-1084-2015
- **Recalling firm:** Oasis Medical, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-04-10
- **Report date:** 2015-05-27
- **Termination date:** 2015-12-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Glendora, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1084-2015

## Citation

> AI Analytics. FDA recall D-1084-2015. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-1084-2015. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
