# FDA recall D-0152-2025

> **Regenerative Processing Plant, LLC** · Class II · drug recall initiated 2024-12-10.

## Product

LITE Regener-Eyes, Ophthalmic Solution (glycerin 0.4%), 3mL bottles, Distributed by: Regener-Eyes, Tampa, FL; Manufactured by: Regenerative Processing Plant, LLC, 34176 US HWY 19N, FL, NDC 82305-006-01

## Reason for recall

Lack of Sterility Assurance

## Distribution

Nationwide within the United States

## Key facts

- **Recall number:** D-0152-2025
- **Recalling firm:** Regenerative Processing Plant, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2024-12-10
- **Report date:** 2024-12-25
- **Termination date:** 2025-06-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Palm Harbor, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0152-2025

## Citation

> AI Analytics. FDA recall D-0152-2025. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/D-0152-2025. Source: US FDA. Licensed CC0.

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