Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
5% DEXTROSE Injection Recalled by Hospira Inc. Due to Lack of Assurance of Sterility: there is a...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Hospira Inc. directly.
Affected Products
5% DEXTROSE Injection, USP, 250 mL ADD-Vantage Unit bag (NDC 0409-7100-02), UPC (01)0030404097100026; packaged in 24 bags per case pack (NDC 0409-7100-02), UPC (01)30304097100027(30)01, Rx ONLY, Hospira, Inc., Lake Forest, IL 60045.
Quantity: 94,440 bags
Why Was This Recalled?
Lack of Assurance of Sterility: there is a potential for solution to leak at the administrative port of the primary container.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Hospira Inc.
Hospira Inc. has 245 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report