US Drug Recall Register
Class I · High risk Terminated Initiated Dec 14, 2018 (8 years ago)

Lubrisine eye drops (polyethylene glycol 400 0.4% and Propylene glycol 0.3%), 30 ML…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

What was recalled

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

Recalling firm
Results RNA, LLC
Origin
UT, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0360-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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