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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K031185
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Plum A+ Single Channel Infusion Pumps with Plug-and-Play Modules that provide wired Ethernet and wir... 2 12/07/2012 Hospira Inc.
Plum A+3 Triple Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold un... 2 10/04/2011 Hospira Inc.
Plum A+3 Triple Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold un... 2 09/29/2011 Hospira Inc.
Plum A+3 Triple Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold un... 2 03/14/2011 Hospira Inc.
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