Medical Device Recalls
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11 to 15 of 15 Results
510(K) Number: K070398 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of ... | 2 | 07/07/2017 |
FEI # 3013319212 ICU |
| The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of ... | 2 | 07/07/2017 |
FEI # 3013319212 ICU |
| Plum A+ Infusion Pump; List Number: 12391; Product Usage: The Plum A+ Infusion Systems are ... | 2 | 11/14/2013 |
FEI # 3013319212 Hospira Inc. |
| The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines ... | 2 | 11/14/2013 |
FEI # 3013319212 Hospira Inc. |
| Plum A+ v.11.X, list #s 12391-04-01, 12391-04-03, 12391-04-05, 12391-04-11, 12391-04-51; AC cord man... | 2 | 10/06/2009 |
FEI # 2921482 Hospira Inc |
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