Eye Drops Recalled Due to Lack of Sterility Assurance
TRP Natural Eyes sterile eye drops are being recalled because the manufacturer cannot assure the product maintains sterility. The recall involves 196,111 units distributed to retailers 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 for a sterile ophthalmic product where the manufacturer cannot assure sterility. Although no illnesses or injuries have been reported, loss of sterility in eye drops represents a potential serious hazard. The score reflects the preventative nature of this recall without confirmed contamination.
Plain-English summary
TRP Natural Eyes, Dryness Relief Sterile Eye Drops (Homeopathic, 0.33 FL OZ/10 mL) is being recalled. The product is manufactured by AMMAN PHARMACEUTICAL INDUSTRIES in Jordan, exclusively for TRP Company, Inc., located at 1575 Delucchi Lane, Reno, Nevada.
The FDA issued this recall because the manufacturer cannot provide assurance that the product maintains its required sterility according to FDA standards.
The recall involves approximately 196,111 units distributed to two direct accounts in Rhode Island and Colorado. The affected lot numbers are IX001 (expiration 07/24) and IX002 (expiration 12/24). The product's National Drug Code (NDC) is 17312-178-15.
The recalled product
- Product
- TRP Natural Eyes, Dryness 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:17312-178-15.
- Manufacturer
- AMMAN PHARMACEUTICAL INDUSTRIES
- Category
- Drug — Ophthalmic / Eye Drops
- Affected units
- 196,111
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 (2)
- Lot: IX001 EXP: 07/24
- Lot: IX002 EXP: 12/24
Distribution
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.
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