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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 Recall Date to: 07/23/2014
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Product Description
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FDA Recall
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Z-0624-2013 - 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 12/31/2012 Hospira Inc.
Z-0626-2013 - Plum A+ Hyperbaric Single Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; list number 11005 Product Usage: The Plum A+ Hyperbaric Infusion System is exclusively designed for hyperbaric t... 2 12/31/2012 Hospira Inc.
Z-0625-2013 - 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 12/31/2012 Hospira Inc.
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