TRP Natural Eyes Floaters Relief — Class II drug recall D-0380-2024
Ongoing recall by Optikem International, Inc., reported 2024-03-20, distributed nationwide. Lack of Assurance of Sterility
| Recall number | D-0380-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Optikem International, Inc., Denver, CO, United States |
| Recall initiated | 2024-02-29 |
| Classified | 2024-03-12 |
| Reported by FDA | 2024-03-20 |
| Distributed | Nationwide (US) |
| Quantity | 24,216 bottles |
| Reason classes | sterility |
| NDC | 17312-0098-15 |
| Lot numbers | F404, F405, F406 |
| Expiration dates | 2025-05-14, 2025-08-24, 2026-10-11 |
Product
TRP Natural Eyes Floaters Relief, Sterile Eye Drops, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-098-15.
Reason for recall
Lack of Assurance of Sterility
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0380-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.