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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls Recall Date to: 07/24/2014
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Product Description
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FDA Recall
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Recalling Firm
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Z-1816-2009 - Hospira Phoenix Infusion System with MedNet Software, Symbiq Two-Channel Infusion System, Software versions v2.1 & v3.0, Manufactured by Hospira Inc., Morgan Hill, CA 2 08/11/2009 Hospira Inc
Z-1815-2009 - Hospira Phoenix Infusion System with MedNet Software, Symbiq One-Channel Infusion System, Software versions v2.1 & v3.0, Manufactured by Hospira Inc., Morgan Hill, CA. 2 08/11/2009 Hospira Inc
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