Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K052578 |
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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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Recovery G2 Filter System - Jugular/Subclavian Delivery Kit, for use in the prevention of recurrent ... | 2 | 02/01/2007 | Bard Peripheral Vascular Inc |
G2 Filter System - Jugular/Subclavian Delivery Kit, for use in the prevention of recurrent pulmonary... | 2 | 02/01/2007 | Bard Peripheral Vascular Inc |
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