Class IIDrug
TRP The Relief Products* Gentle Eyes Lubricant Eye… recall
Summary
Sterling Pharmaceutical Services LLC is recalling TRP The Relief Products* Gentle Eyes Lubricant Eye Drops (drug). According to the FDA report, the reason is: Lack of Assurance of Sterility. The FDA rated this a Class II: the product may cause temporary or medically reversible health problems; serious harm is unlikely. Recall status: Ongoing.
Details from the FDA report
- Product
- TRP The Relief Products* Gentle Eyes Lubricant Eye Drops, Carboxymethylcellulose sodium 0.5%, Sterile Eye Drops, 0.5 FL OZ (15 mL) bottles, Manufactured exclusively for TRP Company, Inc. 1575 Delucci Ln, Reno, NV 89502, NDC 17312-430-15.
- Reason
- Lack of Assurance of Sterility
- Lot / code info
- Lot # 3279, Exp 6/30/2027; Lot # 3292, Exp 5/31/2027.
- Quantity
- 14538 bottles
- Distribution
- USA Nationwide
- Recalling company
- Sterling Pharmaceutical Services LLC, Dupo, IL United States
- Recall started
- August 20, 2026
- FDA report date
- September 30, 2026
- Classification
- Class II: The product may cause temporary or medically reversible health problems; serious harm is unlikely.
- Voluntary / mandated
- Voluntary: Firm initiated
- Status
- Ongoing
- Recall number
- D-0860-2026
What to do
- Check whether you have this product, and compare the lot numbers, codes, or dates on your package with the codes listed above.
- If it matches, stop using it and keep it away from children and pets.
- Contact the recalling company (Sterling Pharmaceutical Services LLC) or the store where you bought it about returns or refunds.
- Do not stop a prescribed medication without first talking to your pharmacist or doctor; they can help find a safe replacement.
- If you think the product made you or someone else sick, contact a doctor or pharmacist. In an emergency call 911.
- You can report problems to the FDA via MedWatch.