The Recall Desk
HighFDA (Drugs)·D-1163-2023·Announced 2023-09-27

TRP Natural Eyes Red Eye Relief Recalled for Sterility Failure

TRP Natural Eyes Red Eye Relief sterile eye drops have been recalled due to lack of assurance of sterility. The recall affects 8,868 units distributed to accounts in Rhode Island and Colorado.

What this means for you

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 an FDA Class II recall of a sterile ophthalmic product with documented lack of sterility assurance. While no illnesses or injuries have been reported, the product represents a risk-of-harm situation through potential microbial contamination of sensitive ocular tissue.

Plain-English summary

TRP Natural Eyes Red Eye Relief, a sterile ophthalmic eye drop product, has been recalled by AMMAN PHARMACEUTICAL INDUSTRIES due to a lack of assurance of sterility during manufacturing. The product is a 0.33 FL OZ (10 mL) homeopathic formulation.

The recall involves 8,868 units bearing lot number FQ001 with an expiration date of 07/24. This lot was distributed to two wholesale accounts in Rhode Island and Colorado.

Any consumers who have this product should discontinue use immediately. The product's lack of confirmed sterility assurance means it may be contaminated and could pose a risk of infection if applied to the eyes. Anyone who has used the product and experiences eye symptoms should consult a healthcare provider.

The recalled product

Product
TRP Natural Eyes, Red Eye Relief, Sterile Eye drops, Homeopathic 0.33 FL OZ (10 mL), Manufactured in Jordan, exclusively for TRP Company, Inc., 1575 Delucchi Lane, Reno, NV 89502, NDC: 17312-058-15.
Manufacturer
AMMAN PHARMACEUTICAL INDUSTRIES
Category
Drug — Ophthalmic / Eye Drops
Hazard
Affected units
8,868

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 (1)

  • Lot: FQ001 EXP:07/24

Distribution

Distributed in 2 states:

Part of a larger recall action

This product is one of 17 recalled by AMMAN PHARMACEUTICAL INDUSTRIES 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 17 products in this recall →

Related recalls

Same manufacturer · AMMAN PHARMACEUTICAL INDUSTRIES

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Same hazard · sterility failure

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