US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 2, 2022 (4 years ago)

Difluprednate Ophthalmic Emulsion 0.05%, For Ophthalmic Use Only, Sterile, 5 mL bottles…

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

Why it was recalled

Lack of Assurance of Sterility: Complaints received of defective container closure.

What was recalled

Difluprednate Ophthalmic Emulsion 0.05%, For Ophthalmic Use Only, Sterile, 5 mL bottles, Manufactured by Cipla Ltd., India, Manufactured for: Cipla USA, Inc., NJ 07059, NDC 69097-341-35.

Recalling firm
Cipla
NDC code
69097-341-35
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1328-2022

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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