Recall RadarFRESHKOTE LUBRICANT EYEDROPS, Sterile, 0.33 FL OZ (10mL), Harrow Eye LLC, Nashville, TN USA.
Lack of Assurance of Sterility
Read the official FDA notice →What to do
Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.
Details
- Recalling company
- Harrow Eye LLC — Nashville, TN
- Severity
- Class II — moderate
- Reported
- April 29, 2026
- Quantity
- 50,900 units
- Recall number
- D-0489-2026
- Status
- Ongoing
- Source
- FDA
Where it went
Nationwide within the United States
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