Class II Recall

CIPLA

Product
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.
Reason
Lack of Assurance of Sterility: Complaints received of defective container closure.
Classification
Class II
Status
Terminated
Lot
Lot # DEG3LC2, Exp 05/2023
Date
Disclaimer: This tool indexes published US FDA drug-enforcement recall records from all countries, limited to the latest five years. A company or product not appearing here is not proof that it is compliant, approved, safe, or free of FDA action.
CIPLA — Class II Recall | MedicineWatch US