Medical Device Recalls
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1 result found
PMA Number: P100013 |
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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, a Johnson and Johnson Company, ExoSeal(TM) 6F Vascular Closure Device, cat. No EX500, EX6... | 2 | 01/25/2013 | Cordis Corporation |
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