Agency classClass IIOur severity:High FDA (Drugs)·D-0381-2024·Announced 2024-03-20

TRP Natural Eyes eye drops recalled due to lack of sterility assurance

TRP Natural Eyes Aging Eye Relief eye drops are being recalled because the manufacturer cannot assure the product meets sterility requirements. The recall affects 19,344 bottles distributed nationwide.

The agency’s classification

FDA (Drugs): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 3/5 (High).

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: This is a risk-of-harm product—eye drops require sterility due to direct contact with sensitive ocular tissue. No illnesses or injuries have been reported, but the lack of sterility assurance represents a serious potential hazard that meets the rubric criterion for high-severity recalls.

Plain-English summary

TRP Natural Eyes Aging Eye Relief, a homeopathic sterile eye drop product, is being recalled by Optikem International, Inc. The recall is due to lack of assurance of sterility—the manufacturer cannot confirm the product meets required sterility standards.

The recall affects 19,344 bottles with lot numbers G806 (expiration 06-01-2025) and G807 (expiration 10-27-2026). The affected product was distributed nationwide in the United States.

Consumers who have purchased this product should stop using it immediately. Anyone with questions or concerns should consult their healthcare provider or pharmacist.

The recalled product

Product: TRP Natural Eyes Aging Eye Relief, Sterile Eye Drops, Homeopathic, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-027-15.
Manufacturer: Optikem International, Inc.
Category: Drug — Eye Drops / Ophthalmic
Hazard: sterility-failure
contamination-risk
Affected units: 19,344

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (4)

Lot #: G806
Exp: 06-01-2025
G807
Exp: 10-27-2026.

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 10 recalled by Optikem International, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 10 products in this recall →

Same manufacturer · Optikem International, Inc.

See all →

High
TRP Blur Relief Eye Drops Recalled Nationwide for Sterility Assurance Failure
FDA (Drugs) · 2024-03-20
High
TRP Natural Eyes Floaters Relief eye drops recalled due to sterility concerns
FDA (Drugs) · 2024-03-20
High
TRP Natural Eyes Allergy Relief Eye Drops Recalled for Sterility Assurance Issues
FDA (Drugs) · 2024-03-20
High
TRP Eye Strain Relief Eye Drops Recalled Due to Lack of Sterility Assurance
FDA (Drugs) · 2024-03-20
High
TRP Natural Eyes Pink Eye Relief Eye Drops Recalled for Sterility Concerns
FDA (Drugs) · 2024-03-20

Same hazard · sterility failure