D-0766-2026 Class II Ongoing
FDA drug recall D-0766-2026 was initiated by Prestige Brands Holdings on July 29, 2026 and is designated Class II. Reason for recall: Lack of assurance of sterility. The recall is due to potential contamination The recall status is ongoing. Affected quantity: 39,060 15mL-bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- August 19, 2026
- Initiation Date
- July 29, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 39,060 15mL-bottles
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
Reason for Recall
Lack of assurance of sterility. The recall is due to potential contamination
Distribution Pattern
Nationwide in the USA.
Code Information
Lot 2552A, Exp 09/30/2027