Class IIDrug
Clear Eyes Maximum Itchy Eye Relief recall
Summary
Prestige Brands Holdings is recalling CLEAR EYES Maximum Itchy Eye Relief (drug). According to the FDA report, the reason is: Lack of assurance of sterility. The recall is due to potential contamination. The FDA rated this a Class II: the product may cause temporary or medically reversible health problems; serious harm is unlikely. Recall status: Ongoing.
Details from the FDA report
- 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
- Lack of assurance of sterility. The recall is due to potential contamination
- Lot / code info
- Lot 2552A, Exp 09/30/2027
- Quantity
- 39,060 15mL-bottles
- Distribution
- Nationwide in the USA.
- Recalling company
- Prestige Brands Holdings, Tarrytown, NY United States
- Recall started
- July 29, 2026
- FDA report date
- August 19, 2026
- Classification
- Class II: The product may cause temporary or medically reversible health problems; serious harm is unlikely.
- Voluntary / mandated
- Voluntary: Firm initiated
- Status
- Ongoing
- Recall number
- D-0766-2026
What to do
- Check whether you have this product, and compare the lot numbers, codes, or dates on your package with the codes listed above.
- If it matches, stop using it and keep it away from children and pets.
- Contact the recalling company (Prestige Brands Holdings) or the store where you bought it about returns or refunds.
- Do not stop a prescribed medication without first talking to your pharmacist or doctor; they can help find a safe replacement.
- If you think the product made you or someone else sick, contact a doctor or pharmacist. In an emergency call 911.
- You can report problems to the FDA via MedWatch.