US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 29, 2022 (4 years ago)

Pataday, Once Daily Relief, Olopatadine hydrochloride ophthalmic solution 0.2%…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: products were stored outside the drug label specifications.

What was recalled

Pataday, Once Daily Relief, Olopatadine hydrochloride ophthalmic solution 0.2%, Antihistamine, Eye Allergy Itch Relief, Once Daily, Sterile, 2.5 mL (0.085 FL OZ) bottle per box, Alcon, NDC 0065-8150-01.

Recalling firm
Mckesson Medical-Surgical Inc. Corporate Office
NDC code
0065-8150-01
Origin
VA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1321-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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