FDA Drug Recalls

Recalls / Class II

Class IID-0380-2024

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.

Affected lot / code info
Lot #: F404, Exp: 05-14-2025, F405, Exp: 08-24-2025, F406, Exp: 10-11-2026.

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
Optikem International, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
2172 S Jason St, N/A, Denver, Colorado 80223-4005

Distribution

Quantity
24,216 bottles
Distribution pattern
Product distributed Nationwide in the USA

Timeline

Recall initiated
2024-02-29
FDA classified
2024-03-12
Posted by FDA
2024-03-20
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0380-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.