# FDA recall D-0523-2016

> **Oasis Medical, Inc.** · Class III · drug recall initiated 2015-10-19.

## Product

HPMC Visoelastic Topical, 8,000 cps,  Reference 5200, 1.5 mL in 3-mL Syringe, OASIS Medical Inc, 514 South Vermont Avenue Glendora, CA 91741

## Reason for recall

Failed pH Specification: It has been determined that the pH of the lots recalled, may not meet specification at expiry.

## Distribution

Nationwide and Saudi Arabia, Israel, Chile, Norway, Ecuador, Greece, Switzerland, Canada, England, Columbia, Poland, South Africa, Germany, Pakistan, El Salvador, Dubai, Belgium

## Key facts

- **Recall number:** D-0523-2016
- **Recalling firm:** Oasis Medical, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-10-19
- **Report date:** 2015-12-30
- **Termination date:** 2016-03-14

- **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-0523-2016

## Citation

> AI Analytics. FDA recall D-0523-2016. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0523-2016. Source: US FDA. Licensed CC0.

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