Class II

Drug Recall: FRESHKOTE LUBRICANT EYEDROPS, Sterile, 0.33 FL OZ (10mL), Harrow Eye LLC, Nashville, TN USA.

Harrow Eye LLC · April 17, 2026

Reason for Recall

Lack of Assurance of Sterility

Distribution

Nationwide within the United States

States Affected

NATIONWIDE

Quantity Affected

50,900 units

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0489-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.