Regenerative Processing Plant, LLC: Drug Recall

Recall #D-0152-2025 · 12/10/2024

Class II: Risk

Recall Details

Recall Number: D-0152-2025
Classification: Class II
Product Type: Drug
Recalling Firm: Regenerative Processing Plant, LLC
Status: Terminated
Date Initiated: 12/10/2024
Location: Palm Harbor, FL, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 170812 bottles

Reason for Recall

Lack of Sterility Assurance

Product Description

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

Distribution Pattern

Nationwide within the United States

Other Recalls by Regenerative Processing Plant, LLC

Class II: Risk 12/10/2024

Lack of Sterility Assurance

View all recalls by Regenerative Processing Plant, LLC →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.