Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K021350 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Plum A+3 Infusion Pump System; List Number: 12348; Product Usage: The Plum A+ Infusion Syst... | 2 | 11/14/2013 | Hospira Inc. |
Plum A+3 Triple Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold un... | 2 | 12/31/2012 | Hospira Inc. |
Plum A+3, list #s 12348-04-03, 12348-04-05, 12348-04-07, 12348-04-51; AC cord manufactured by Electr... | 2 | 10/06/2009 | Hospira Inc |
The Hospira Plum A+ I.V. Infusion pump is a cassette-based, multi-function fluid delivery infusion s... | 2 | 01/27/2005 | Hospira Inc |
The Hospira Plum A+3 I.V. Infusion pump is a cassette-based, multi-function fluid delivery infusion ... | 2 | 01/27/2005 | Hospira Inc |
The Plum A+3 Infusion System is a cassette based multifunction infusion system that allows two lines... | 2 | 11/14/2013 | Hospira Inc. |
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