Medical Device Recalls
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11 to 17 of 17 Results
510(K) Number: K042081 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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+ Single Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold und... | 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. |
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+ Infusion System with Hospira Mednet, list #s 20679-04-01, 20679-04-03, 20679-04-05, 20679-04... | 2 | 10/06/2009 | 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 |
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