Medical Device Recalls
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81 to 81 of 81 Results
510(K) Number: K072642 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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"***BIOMET 3i***4555 Riverside Drive Palm Beach Gardens FL 33410 USA***REF SWCA62***Conical Abutment... | 2 | 11/03/2011 | Biomet 3i, LLC |
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