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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 19 of 19 Results
510(K) Number: K042081
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Product Description
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Recall
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FDA Recall
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Plum A+ Single Channel Infusion Pumps with Hospira Mednet Software and a Connectivity Engine periphe... 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+ Single Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold und... 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+ Single Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold und... 2 09/29/2011 Hospira Inc.
Plum A+ Single Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold und... 2 03/14/2011 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.
Plum A+3 Infusion System with Hospira Mednet, list # 20678-04-01, 20678-04-03, 20678-04-51, 20678-04... 2 10/06/2009 Hospira Inc
Plum A+ Infusion System with Hospira Mednet, list #s 20679-04-01, 20679-04-03, 20679-04-05, 20679-04... 2 10/06/2009 Hospira Inc
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