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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Topical Products

Results RNA, LLC: Lubrisine Eye Drops Recalled for Sterility Issues and Undeclared Ingredients

Agency Publication Date: December 20, 2018
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Summary

Results RNA, LLC is recalling 10,297 bottles of Lubrisine eye drops (polyethylene glycol 400 0.4% and propylene glycol 0.3%) because the product lacks sterility assurance and contains undeclared colloidal silver. The recall affects all lots of the 30 ML bottles distributed nationwide. Because these are eye drops, a lack of sterility poses a serious risk of infection, and the presence of undeclared ingredients like colloidal silver can cause further adverse reactions. Consumers should contact their healthcare provider or pharmacist regarding the use of this product.

Risk

A lack of sterility in eye drops can introduce bacteria directly into the eye, potentially leading to severe infections or permanent vision loss. Additionally, the undeclared presence of colloidal silver may cause unintended side effects or allergic reactions in sensitive individuals.

What You Should Do

  1. Check your medicine cabinet for 30 ML bottles of Lubrisine eye drops (polyethylene glycol 400 0.4% and Propylene glycol 0.3%) with UPC 7 9238230723 4.
  2. Verify if you have any lot of this product, as 'All Lots' are currently included in this recall.
  3. Stop using the eye drops immediately and contact your healthcare provider or pharmacist for guidance regarding any potential health concerns or alternative treatments.
  4. Return any unused bottles of Lubrisine eye drops to the place of purchase for a refund.
  5. Contact Results RNA, LLC at their Orem, Utah facility or through their official website for further instructions regarding the recall.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Refund and Healthcare Consultation

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Lubrisine eye drops (polyethylene glycol 400 0.4% and Propylene glycol 0.3%) (30 ML)
Model:
D-0360-2019
UPC Codes:
792382307234
Lot Numbers:
All Lots

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 81742
Status: Resolved
Manufacturer: Results RNA, LLC
Sold By: Results RNA, LLC
Manufactured In: United States
Units Affected: 10,297 bottles
Distributed To: Nationwide
Agency Last Updated: January 14, 2019

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.