Medical Device Recalls
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1 result found
510(K) Number: K962230 |
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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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B. Braun Celsite® Venous Access Ports , Distributed by Aesculpa Inc. Model ST301, ST305V, ST301G,... | 2 | 06/27/2011 | B. Braun Interventional Systems |
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