Class II Recall

Akorn, Inc

Product
PrednisoLONE Oral Solution USP, 15 mg per 5 mL, 240 ml bottle, Rx Only, HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC: 50383-042-24
Reason
Defective Container: Product has incomplete induction seals.
Classification
Class II
Status
Ongoing
Lot
Lot# 379804, Exp. 8/31/2023
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.
Akorn, Inc — Class II Recall | MedicineWatch US