FDAFDA · Food and drugs·Recall number D-0489-2026
FRESHKOTE LUBRICANT EYEDROPS, Sterile, 0.33 FL OZ (10mL), Harrow Eye LLC, Nashville, TN USA.
Published April 29, 2026 · Recall initiated: April 17, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Harrow Eye LLC
- Distributor
- Nationwide within the United States
- Lot
- Lot #: 1X68, 1X69, Exp. Date 05/31/2027.
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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