Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) , 0.5
Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company
Summary
The FDA issued a Class II for Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, by Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company. Reason: Lack of Assurance of Sterility.
Details
Source
Drug Recall
External ID
D-0870-2026
Action Date
2026-09-30
Status
Ongoing
Category
drug
Product Description
Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) , 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15
Lot/Code Info: Lot #: RL25G02, RL25G03, RL25G04, Exp. Date Jul-27; RL25H02, RL25H03, RL25H04, Exp. Date Aug-27; RL25K01, RL25K02, RL25K03, RL25K04, Exp. Date Sep-27; RL25M01, RL25M02, RL25M03, RL25M04, Exp. Date Oct-27; RL25N01, RL25N02, RL25N04, Exp. Date Nov-27.
Quantity Affected: 2,356,248 bottles
Reason for Recall
Lack of Assurance of Sterility
Distribution
Nationwide in the USA.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-09-15
Company
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 26 drug recalls issued in the same week, part of 66 drug-related FDA actions this month.
Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company have FDA actions?
Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0870-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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