TRP Natural Eyes Pink Eye Relief Eye Drops Recalled for Sterility Concerns
TRP Natural Eyes Pink Eye Relief sterile eye drops are being recalled due to lack of assurance of sterility. The recall affects 139,656 bottles distributed nationwide.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
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 due to lack of assurance of sterility. No illnesses or injuries have been reported, but the product presents a risk of harm if not sterile, fitting the High category for risk-of-harm products without reported injury.
Plain-English summary
Optikem International, Inc. is recalling TRP Natural Eyes Pink Eye Relief sterile eye drops (homeopathic, 0.33 FL OZ / 10 mL bottles) due to lack of assurance of sterility. The recalled product includes lots P516 through P526 with expiration dates ranging from March 2024 through June 2026.
The product has been distributed nationwide in the USA. Affected consumers should stop using the product and may contact the manufacturer or their healthcare provider with questions.
The recalled product
- Product
- TRP Natural Eyes Pink Eye Relief, Sterile Eye Drops, Homeopathic, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-013-15.
- Manufacturer
- Optikem International, Inc.
- Category
- Drug — Ophthalmic
- Hazard
- Affected units
- 139,656
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 (20)
- Lot #: P516
- Exp: 03-24-2024
- P517
- Exp: 08-31-2024
- P518
- Exp:10-20-2024
- P519
- Exp: 03-09-2025
- P520
- Exp: 10-19-2025
- P521
- Exp: 11-09-2025
- P522
- Exp: 11-16-2025
- P523
- Exp: 01-18-2026
- P524
- Exp: 04-26-2026
- P525
- Exp: 05-10-2026
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.
See all 10 products in this recall →Related recalls
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