CLASS II ONGOING Drug recall · Reported 20 Mar 2024 · FDA Enforcement Report

TRP Eye strain Relief, Sterile Eye Drops, Homeopathic recalled

Optikem International is recalling TRP Eye strain Relief, Sterile Eye Drops, Homeopathic, distributed nationwide in the US. The recall was initiated on 29 Feb 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: E206, Exp: 09-21-2025
Quantity recalled10,536 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0379-2024
FDA event ID
94145
Recalling firm
Optikem International, Denver, CO
Classification
Class II
Status
Ongoing
Recall initiated
29 Feb 2024
FDA classified
12 Mar 2024
Reported
20 Mar 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility
Drug class
Eye Drops

Timeline

29 Feb 2024Recall initiated by company
12 Mar 2024Classified by FDA+12 days
20 Mar 2024Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Lack of Assurance of Sterility

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

TRP Eye strain Relief, Sterile Eye Drops, Homeopathic, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-172-15.

Where it was distributed

Product distributed Nationwide in the USA

Nationwide

Questions about this recall

Is TRP Eye strain Relief, Sterile Eye Drops, Homeopathic recalled?

Yes. Optikem International recalled TRP Eye strain Relief, Sterile Eye Drops, Homeopathic on 29 Feb 2024. The recall is Class II and its status is Ongoing. Recall number D-0379-2024.

Why was it recalled?

Lack of Assurance of Sterility

Which lots are affected?

Lot #: E206, Exp: 09-21-2025

Where was it sold?

Product distributed Nationwide in the USA

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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