Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DOBUTamine Injection Recalled by Hospira Inc. Due to Discoloration: Firm received complaints of product discoloration and...
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
DOBUTamine Injection, USP 250 mg/20 mL, 20 mL Vial, For IV Use Only, Must be Diluted Prior to Use, (12.5 mg per mL), Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-2025-20
Quantity: 24000 vials
Why Was This Recalled?
Discoloration: Firm received complaints of product discoloration and particulates.
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