MedicineWatch US
Class II Recall

Fresenius Kabi USA, LLC

Product
5% Dextrose Injection, USP 5 g per 100 mL (50 mg per mL) 100 mL in a 100 mL freeflex bag, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Use NDC: 65219-464-05, Unit of Sale NDC Number: 65219-464-50.
Reason
Lack of Assurance of Sterility
Classification
Class II
Status
Ongoing
Lot
Batch# 6402399, 6402400, 6402401, Exp Date: 02/28/2027.
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.
Fresenius Kabi USA, LLC — Class II Recall | MedicineWatch US