Harrow Eye LLC recalls FRESHKOTE LUBRICANT EYEDROPS, Sterile, 0.33 FL OZ (10mL), Harrow Eye LLC, Nashville, TN USA.
Recalled April 29, 2026 · FDA recall D-0489-2026 · Harrow Eye
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
50,900 units
Sold at
Nationwide within the United States
Description
Lack of Assurance of Sterility
Product
FRESHKOTE LUBRICANT EYEDROPS, Sterile, 0.33 FL OZ (10mL), Harrow Eye LLC, Nashville, TN USA.
Manufacturer(s)
Harrow Eye LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →