Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Diazepam Injection USP 10mg/2mL (5 mg/mL Recalled by Hospira Inc. Due to Crystallization: Product contains particulate identified to be crystallized...
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
Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32
Quantity: 373,850 tubes
Why Was This Recalled?
Crystallization: Product contains particulate identified to be crystallized active ingredient.
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