Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
METRONIDazole Injection Recalled by Hospira Inc. Due to Lack of Assurance of Sterility: There is the...
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
METRONIDazole Injection, USP 500 mg (5 mg/mL), 100 mL Bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 (NDC 0409-7811-24)
Quantity: 567,624 bags
Why Was This Recalled?
Lack of Assurance of Sterility: There is the potential for the solution to leak from the administrative port to the fill tube seal.
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