Warning
Prestige Brands Holdings Recalls CLEAR EYES Maximum Itchy Eye Relief
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #D-0766-2026Drug / Pharmaceutical
Prestige Brands Holdings Recalls CLEAR EYES Maximum Itchy Eye Relief
Prestige Brands Holdings · Class II — Moderate Risk
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
FDA Classification
Class II — Moderate Risk
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.
Distribution
Nationwide in the USA.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
Prestige Brands Holdings has recalled a pharmaceutical product that the FDA classified as Class II affecting 39,060 15mL-bottles. The recall was initiated on July 29, 2026. Lack of assurance of sterility. The recall is due to potential contamination. It was distributed nationwide. Class II recalls involve products that might cause a temporary health problem or pose only a slight threat of a serious nature. Consumers should discontinue use and contact the firm.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medical Product Contamination.