Company: Hospira Inc.
Date of Enforcement Report: 8/7/2013
Class ll:

PRODUCT

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. Recall Number Z-1847-2013

REASON
The devices secondary audio signal fails to activate.

RECALLING FIRM/MANUFACTURER
Hospira Inc., Lake Forest, IL on 2/4/2013. Voluntary: Firm Initiated recall is ongoing.

VOLUME OF PRODUCT IN COMMERCE
2,791 units

DISTRIBUTION
Nationwide

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