# FDA recall D-0384-2024

> **Optikem International, Inc.** · Class II · drug recall initiated 2024-02-29.

## Product

hyalogic For Dry Eyes, HylaTears", Lubricant Eye Drops, 0.67 FL OZ (20mL) bottle, Manufactured for hyalogic, 610 NW Platte Valley Dr., Riverside, MO 64150

## Reason for recall

Lack of Assurance of Sterility

## Distribution

Product distributed Nationwide in the USA

## Key facts

- **Recall number:** D-0384-2024
- **Recalling firm:** Optikem International, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2024-02-29
- **Report date:** 2024-03-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Denver, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0384-2024

## Citation

> AI Analytics. FDA recall D-0384-2024. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/D-0384-2024. Source: US FDA. Licensed CC0.

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