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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
Related Medical Device Recalls Date Classified to: 04/20/2014
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Product Description
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Recall
Class
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Date
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Recalling Firm
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Z-0009-2012 - Plum A+ Single Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold under the following configurations: a) list 11971 b) list 11973 - software version 10.3 c) list 12391 -... 2 Oct-04-2011 Hospira Inc.
Z-0011-2012 - Plum A+ Hyperbaric Single Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; list 11005 Product Usage: The Plum A+ Hyperbaric Infusion System is exclusively designed for hyperbaric t... 2 Oct-04-2011 Hospira Inc.
Z-0010-2012 - Plum A+3 Triple Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold under the following configurations: a) list 12348 - software version 10.3; b) list 12618 - software ve... 2 Oct-04-2011 Hospira Inc.
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