TRP Natural Eyes Red Eye Relief eye drops recalled due to sterility concerns
TRP Natural Eyes Red Eye Relief PF sterile eye drops are being recalled due to lack of assurance of sterility. Approximately 196,442 units distributed to accounts in Rhode Island and Colorado may be 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 with no reported illnesses or injuries, and the hazard is theoretical (lack of assurance of sterility) rather than confirmed contamination. It meets the rubric for Score 3 as a risk-of-harm product where injury has not yet been reported.
Plain-English summary
TRP Natural Eyes Red Eye Relief PF is a homeopathic sterile eye drop product in 0.33 FL OZ (10 mL) bottles, manufactured in Jordan by Amman Pharmaceutical Industries for TRP Company, Inc., located at 1575 Delucchi Lane, Reno, NV 89502. The product has NDC 17312-095-19. The affected lots are IW001 (expiration 07/24) and Lot IW002 (expiration 12/24).
The recall was issued due to lack of assurance of sterility. This means the manufacturer cannot guarantee that the product meets sterility requirements. Sterility is critical for eye drop products, as non-sterile products applied to the eye can introduce harmful microorganisms.
Approximately 196,442 units were distributed to two direct accounts in Rhode Island and Colorado.
Consumers should not use this product if they have the recalled lots. Those who have used it and have concerns should contact a healthcare provider.
The recalled product
- Product
- TRP Natural Eyes, Red Eye 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: 17312-095-19.
- Manufacturer
- AMMAN PHARMACEUTICAL INDUSTRIES
- Category
- Drug — Ophthalmic / Eye drops
- Hazard
- Affected units
- 196,442
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: IW001 EXP:07/24
- Lot: IW002 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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