Recalls / Class II

Class IID-0376-2024

Product

TRP Blur Relief, Sterile Eye Drops, Homeopathic 0.5 FL OZ (15mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-002-11.

Affected lot / code info

Lot #: B905, Exp: 07-13-2025

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

7,248 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-0376-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.