Class II Recall

Akorn, Inc.

Product
Levofloxacin Injection 500mg/20 mL (25 mg/mL), For Intravenous Infusion, packaged in a) 20mL vials and b) 30 mL vials, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. ALL NDCs
Reason
CGMP Deviations: Firm went out of business and could no longer continue stability studies.
Classification
Class II
Status
Ongoing
Lot
All Lots
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