Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The Hospira Symbiq Infusion System is intended for the delivery of fluids Recalled by Hospira Inc. Due to The devices secondary audio signal fails to activate.
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
The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents, nutritionals, electrolytes, blood and blood products via parenteral, enteral, intravenous, intra-arterial, subcutaneous, epidural, or irrigation routes of administration.
Quantity: 2,791 units
Why Was This Recalled?
The devices secondary audio signal fails to activate.
Where Was This Sold?
This product was distributed to 22 states: AL, CA, CT, DE, FL, HI, IL, IN, IA, LA, ME, MD, MA, MI, MN, NJ, NY, NC, PA, SD, TX, WA
About Hospira Inc.
Hospira Inc. has 245 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report