Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K091077 |
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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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Cordis OPTEASE Vena Cava Filter Is indicated for use in the prevention of recurrent pulmonary emb... | 2 | 10/25/2013 | Cordis Corporation |
Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***REF Cat. No.***466F220A and 466F220B***Ve... | 1 | 08/07/2013 | Cordis Corporation |
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