Medical Device Recalls
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1 result found
510(K) Number: K193038 |
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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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| Comprehensive Shoulder Stem, Comprehensive Micro Stem, Comprehensive Mini Stem; uncemented shoulder ... | 2 | 03/20/2025 |
FEI # 3012319330 ZIMMER ORTHOPEDICS MANFACTURING LIMITED-GALWAY |
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