Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K052052 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving ... | 1 | 02/23/2015 | Hospira Inc. |
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