Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K070925 |
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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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| DePuy Mitek Lupine Loop Rapide w/ Orthocord Catalog #210711 The LUPINE BR Anchor System is in... | 2 | 11/30/2011 |
FEI # 1221934 DePuy Mitek, Inc., a Johnson & Johnson Co. |
| Lupine BR Anchor w/Orthocord TCP/PLGA Absorbable Anchor, size 2 (5 metric) Braided Composite Suture,... | 2 | 09/17/2008 |
FEI # 1221934 DePuy Mitek, Inc., a Johnson & Johnson Co. |
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