Sterile Eye Drops Recalled for Lack of Sterility Assurance TRP Natural Eyes
TRP Natural Eyes sterile eye drops have been recalled because their sterility cannot be confirmed. About 8,000 units distributed to medical accounts in Rhode Island and Colorado are affected.
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 lack of assured sterility, posing potential risk of microbial contamination. No illnesses or injuries have been reported in the source material. Per rubric criteria, Class II recalls without hospitalization or reported illness receive a High severity score.
Plain-English summary
TRP Natural Eyes sterile eye drops have been recalled due to lack of assurance of sterility. The product, manufactured in Jordan by AMMAN PHARMACEUTICAL INDUSTRIES for TRP Company, Inc., is a homeopathic eye drop formulation in 0.33 FL OZ bottles designed for eye lid relief.
The recall was initiated because the product cannot be confirmed to meet required sterility standards. This poses a potential risk of microbial contamination, which could lead to eye infections when the product is applied.
Approximately 8,000 units with lot number FV005 and expiration date 03/25 were distributed to two direct accounts in Rhode Island and Colorado. The product is identified by NDC 17312-417-19.
Consumers who have this product should discontinue use immediately. Anyone who has used this product and experiences eye irritation or infection should seek medical attention.
The recalled product
- Product
- TRP Natural Eyes, Eye Lid Relief PF, 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: 17312-417-19.
- Manufacturer
- AMMAN PHARMACEUTICAL INDUSTRIES
- Category
- Drug — Eye Drops / Ophthalmic
- Hazard
- lack-of-sterility-assurance
- microbial-contamination
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: FV005 EXP:03/25
Distribution
Distributed in 2 states:
- CO
- RI
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