Medical Device Recalls
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1 result found
510(K) Number: K071934 |
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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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Biomet Marrowstim Concentration Kit w/single Disposable Separator, Bone Marrow Needle, and 30 ml ACD... | 3 | 04/17/2009 | Biomet, Inc. |
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