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.
Reported: August 7, 2013 Initiated: February 4, 2013 #Z-1847-2013
Product Description
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.
Reason for Recall
The devices secondary audio signal fails to activate.
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 2,791 units
- Distribution
- US Distribution including the states of AL, CA, CT, DE, FL, HI, IA, IL, IN, LA, MA, MD, ME, MI, MN, NC, NJ, NY, PA, SD, TX and WA.
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Hospira Inc.. Units affected: 2,791 units.
Why was this product recalled? ▼
The devices secondary audio signal fails to activate.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 7, 2013. Severity: Moderate. Recall number: Z-1847-2013.
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