Class I โ€” Serious Health Hazard

Serious health hazard โ€” there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Lubrisine eye drops (polyethylene glycol 400 0.4% and Propylene glycol 0.3%) Recalled by Results RNA, LLC Due to Undeclared Excipient

Date: December 14, 2018
Company: Results RNA, LLC
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Results RNA, LLC directly.

Affected Products

Lubrisine eye drops (polyethylene glycol 400 0.4% and Propylene glycol 0.3%), 30 ML bottle, Manufactured and Distributed by: Results RNA, LLC, 1272 S 1380 W., Orem, UT 84058, UPC 7 9238230723 4

Quantity: 10,297 bottles

Why Was This Recalled?

Lack of Sterility Assurance and Incorrect/Undeclared excipient: Product was found to contain undeclared colloidal silver

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Results RNA, LLC

Results RNA, LLC has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report