Recall
FDAHealthMarch 11, 2026

Fresenius Kabi USA, LLC — 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 S

⚠️ Lack of Assurance of Sterility

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
March 11, 2026

US Nationwide , Alaska, and Puerto Rico.

What's affected?

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.
Lot code
Batch# 6402296, Exp Date: 07/31/2026.

Additional details

Batch# 6402296, Exp Date: 07/31/2026.

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated

View original FDA notice →

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