The Recall Desk
HighFDA (Drugs)·D-1158-2023·Announced 2023-09-27

TRP Natural Eyes Eye Ointment Recalled for Lack of Sterility Assurance

TRP Natural Eyes sterile eye ointment (NDC 17312-165-13, Lot 180001, EXP 01/25) is being recalled due to lack of assured sterility. The product was 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: FDA Class II recall for a sterile eye product where sterility cannot be assured. While no illnesses or injuries have been reported, this is a risk-of-harm product where contamination could cause serious eye infection, fitting the rubric criterion for score 3: 'risk-of-harm products where injury has not yet been reported.'

Plain-English summary

TRP Natural Eyes, Eye Lid Relief sterile eye ointment is being recalled due to a lack of assurance of sterility. The product was manufactured in Jordan by AMMAN PHARMACEUTICAL INDUSTRIES exclusively for TRP Company, Inc., located in Reno, Nevada.

The recalled product is identified by NDC 17312-165-13 and comes in 0.14 oz (4 gram) units. The affected lot is 180001 with an expiration date of 01/25. A total of 16,500 units were distributed to two direct accounts in Rhode Island and Colorado.

Because sterility cannot be assured, the product should not be used. Consumers who have purchased TRP Natural Eyes should discontinue use and contact their retailer or TRP Company, Inc. for instructions on how to safely return or dispose of the product.

The recalled product

Product
TRP Natural Eyes, Eye Lid Relief, Sterile Eye ointment, Homeopathic 0.14 oz (4 grams), Manufactured in Jordan, exclusively for TRP Company, Inc., 1575 Delucchi Lane, Reno, NV 89502, NDC: 17312-165-13.
Manufacturer
AMMAN PHARMACEUTICAL INDUSTRIES
Category
Drug — Ophthalmic
Hazard
Affected units
16,500

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: 180001 EXP: 01/25

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 →

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Same manufacturer · AMMAN PHARMACEUTICAL INDUSTRIES

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Same hazard · contamination risk

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