FDAFDA recall D-0766-2026 · Aug 19, 2026
Prestige Brands Holdings: CLEAR EYES Maximum Itchy Eye Relief recall
Recall found
Product
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
Reason for recall
Lack of assurance of sterility. The recall is due to potential contamination
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Lot 2552A, Exp 09/30/2027
- Quantity
- 39,060 15mL-bottles
- Distribution
- Nationwide in the USA.
- Recalling firm
- Prestige Brands Holdings, Tarrytown, NY
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-07-29
Source: openFDA enforcement record D-0766-2026 · search recall number D-0766-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.