Drug recall D-0435-2026
Product
5% Dextrose Injection, USP 2.5 g per 50 mL (50 mg per mL) 50 mL in a 100 mL freeflex bag, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Use NDC: 65219-456-05, Unit of Sale NDC Number: 65219-456-60.
Reason for recall
Lack of Assurance of Sterility
Lots and codes
Batch# 6402296, Exp Date: 07/31/2026.
Recall details
- Recalling firm
- Fresenius Kabi USA, LLC, Lake Zurich, IL
- Distribution
- US Nationwide , Alaska, and Puerto Rico.
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 11, 2026
Related products
- Dextrose – drug information
- NDC 65219-458 Dextrose · Dextrose Monohydrate 50 mg/mL · FRESENIUS KABI USA, LLC
- NDC 65219-456 Dextrose · Dextrose Monohydrate 50 mg/mL · FRESENIUS KABI USA, LLC
- NDC 65219-464 Dextrose · Dextrose Monohydrate 50 mg/mL · FRESENIUS KABI USA, LLC
- NDC 65219-462 Dextrose · Dextrose Monohydrate 50 mg/mL · FRESENIUS KABI USA, LLC
- NDC 65219-460 Dextrose · Dextrose Monohydrate 50 mg/mL · FRESENIUS KABI USA, LLC