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+ Single Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold und... | 2 | 10/04/2011 | 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+ Single Channel Infusion Pumps with Hospira Mednet Software and a Connectivity Engine periphe... | 2 | 12/07/2012 | 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+ Infusion System with Hospira MedNet List 20792-04-25, Pole Clamp Assembly Part Number 820-95... | 2 | 02/04/2015 | Hospira Inc. |
*** 1) Plum A+ Infusion Pump; List Number: 20678; Labeled in part: PLUM A+3; for use with Ho... | 2 | 11/14/2013 | Hospira Inc. |
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