TRP Natural Eyes Floaters Relief eye drops recalled due to sterility concerns
Optikem International is recalling TRP Natural Eyes Floaters Relief eye drops nationwide due to lack of assurance of sterility in manufacturing. Affected bottles have lot numbers F404, F405, or F406.
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 involving lack of sterility assurance in an ophthalmic product that directly poses a risk of eye infection. No illnesses or injuries have been reported. Per the rubric, this qualifies as a risk-of-harm product where injury has not yet been reported, warranting a score of 3 (High).
Plain-English summary
TRP Natural Eyes Floaters Relief, a sterile eye drop product (0.33 FL OZ/10 mL bottles), manufactured by Optikem International, Inc., is being recalled. The recall affects 24,216 bottles distributed nationwide in the United States.
The product is being recalled due to lack of assurance of sterility. The manufacturer was unable to provide adequate assurance that the manufacturing process maintained sterility standards for this ophthalmic product.
Consumers who have purchased this product should stop using it immediately. Affected bottles contain lot numbers F404 (expiration 05-14-2025), F405 (expiration 08-24-2025), or F406 (expiration 10-11-2026). If you have used this product and experience any symptoms of eye irritation or infection, consult with an eye care professional.
The recalled product
- Product
- TRP Natural Eyes Floaters Relief, Sterile Eye Drops, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-098-15.
- Manufacturer
- Optikem International, Inc.
- Category
- Drug — Ophthalmic / Eye Drops
- Affected units
- 24,216
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 (6)
- Lot #: F404
- Exp: 05-14-2025
- F405
- Exp: 08-24-2025
- F406
- Exp: 10-11-2026.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 10 recalled by Optikem International, Inc. 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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