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
___________________________________
