July 2026 FDA Recall Clear Eyes Maximum Itchy Eye Relief by Prestige Brands Holdings
D-0766-2026 - Lack of assurance of sterility. The recall is due to potential contamination

This Class II drug recall was voluntarily initiated by Prestige Brands Holdings on July 29, 2026 for the product Clear Eyes Maximum Itchy Eye Relief. The FDA reported the reason for recall as lack of assurance of sterility. the recall is due to potential contamination. The product was distributed Nationwide and the recall is currently ongoing.

Recall Number: D-0766-2026

Reason for Recall
Lack of assurance of sterility. The recall is due to potential contamination
Initiated
07-29-2026
Reported
08-19-2026
Quantity
39,060 15mL-bottles

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Prestige Brands Holdings
Nationwide in the USA.
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

Batch or Lot Expiration Information

Lot# Lot 2552A, Exp 09/30/2027