CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarr
Summary
The FDA issued a Class II for CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Steri by Prestige Brands Holdings. Reason: Lack of assurance of sterility. The recall is due to potential contamination.
Details
Source
Drug Recall
External ID
D-0766-2026
Action Date
2026-08-19
Status
Ongoing
Category
drug
Product Description
CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Company. NDC: 67172-999-01 UPC 6 78112 65920 3
Lot/Code Info: Lot 2552A, Exp 09/30/2027
Quantity Affected: 39,060 15mL-bottles
Reason for Recall
Lack of assurance of sterility. The recall is due to potential contamination
Distribution
Nationwide in the USA.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-07-29
Company
Tarrytown, NY
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 28 drug recalls issued in the same week, part of 68 drug-related FDA actions this month.
Prestige Brands Holdings has 2 FDA actions in our database, including 2 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 (Prestige Brands Holdings) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Prestige Brands Holdings have FDA actions?
Prestige Brands Holdings has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0766-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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