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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K120121
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate With Taper Adapter-indicated for pr... 2 03/31/2020 Biomet, Inc.
Comprehensive Reverse Shoulder System Glenosphere Mini Baseplate with Taper Adapter, Model Number 01... 2 03/01/2019 Zimmer Biomet, Inc.
Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor, Part Number: 01... 2 02/24/2015 Biomet, Inc.
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