Why it was recalled
Lack of assurance of sterility. The recall is due to potential contamination
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 numbers, UPCs & expiration codes
Lot 2552A, Exp 09/30/2027
Where it was sold
Nationwide in the USA.
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0766-2026
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Jul 29, 2026
- FDA report date
- Aug 19, 2026
- Quantity
- 39,060 15mL-bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Prestige Brands Holdings
Original FDA data
Every field from FDA enforcement report D-0766-2026, exactly as published.
Show all FDA fields
- City
- Tarrytown
- State
- NY
- Status
- Ongoing
- Country
- United States
- Event ID
- 99532
- Address
- 660 White Plains Rd
- Code information
- Lot 2552A, Exp 09/30/2027
- Postal code
- 10591-5139
- Report date
- Aug 19, 2026
- Product type
- Drugs
- Recall number
- D-0766-2026
- Classification
- Class II
- Recalling firm
- Prestige Brands Holdings
- Product quantity
- 39,060 15mL-bottles
- Reason for recall
- Lack of assurance of sterility. The recall is due to potential contamination
- Voluntary / mandated
- Voluntary: Firm initiated
- 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
- Distribution pattern
- Nationwide in the USA.
- Recall initiation date
- Jul 29, 2026
- Initial firm notification
- Letter
- Center classification date
- Aug 14, 2026