Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K132239 |
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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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Central Screw 6.5x25mm - Product Usage: used as a sterile screw that is intended for implantable sho... | 2 | 02/17/2021 | Biomet, Inc. |
Comprehensive Reverse Shoulder System, Item numbers 115394, 115395, 115396, 115398, 180550, 180551, ... | 2 | 12/17/2020 | Biomet, Inc. |
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