Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
25% Dextrose Injection Recalled by Pfizer Inc. Due to Labeling: Incorrect or Missing Lot and/or expiration date....
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
25% Dextrose Injection, USP 2.5 grams (250 mg/mL) 10 mL Single-dose, Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-1775-10
Quantity: 77,100 syringes
Why Was This Recalled?
Labeling: Incorrect or Missing Lot and/or expiration date.
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