Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.
Classification
Class II
Status
Terminated
Lot
Lot # DNC0814A, DNC0815A, Exp. Date 04/2023
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.
SUN PHARMACEUTICAL INDUSTRIES INC — Class II Recall | MedicineWatch US