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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: 04/25/2015
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Product Description
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FDA Recall
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Z-3284-2011 - 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 1... 2 09/29/2011 Hospira Inc.
Z-3286-2011 - Plum A+ Hyperbaric Single Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; list 11005. Hospira has received reports of incorrect seating of the regulator closer on the Plum A+ Infusion... 2 09/29/2011 Hospira Inc.
Z-3285-2011 - 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 - softwar... 2 09/29/2011 Hospira Inc.
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