FDA Class II · Drug · April 29, 2026
FRESHKOTE LUBRICANT EYEDROPS recall — Harrow Eye LLC
Lack of Assurance of Sterility
Official ID D-0489-2026 · Official record ↗
Recall found. Harrow Eye is named in FDA Class II recall D-0489-2026 covering FRESHKOTE LUBRICANT EYEDROPS. Hazard: Lack of Assurance of Sterility Identifying details: Lot #: 1X68, 1X69, Exp. Date 05/31/2027.. Status: Ongoing.
Lack of Assurance of Sterility
Official ID D-0489-2026 · Official record ↗
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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.