Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K141910 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Bio-CORE Cannula (Needle) Set | 2 | 04/02/2015 | Biologic Therapies, Inc |
| Bio-MAC Cannula (Needle) Set | 2 | 04/02/2015 | Biologic Therapies, Inc |
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