Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K083019 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| GemStar SP Infusion Suite Database, Version 1.0; an Rx PC software application; Hospira, Inc., Lake ... | 2 | 04/15/2011 |
FEI # 3013319212 Hospira Inc. |
| The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the ... | 1 | 04/30/2013 |
FEI # 3013319212 Hospira Inc. |
| The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the ... | 1 | 11/21/2013 |
FEI # 3013319212 Hospira Inc. |
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