Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
5% Dextrose Injection Recalled by Pfizer Inc. Due to Lack of sterility assurance: bag has the potential...
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 Pfizer Inc. directly.
Affected Products
5% Dextrose Injection, USP, 50 mL ADD-Vantage Unit, Rx only, Distributed by Hospira, INC., Lake Forest, IL 60045 USA, NDC 0409-7100-68/0409-7100-66
Quantity: 765 bags
Why Was This Recalled?
Lack of sterility assurance: bag has the potential to leak.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Pfizer Inc.
Pfizer Inc. has 114 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report