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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: K053274
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Anatomical Shoulder" Inverse Humeral Cup 2 11/06/2012 Zimmer, Inc.
Anatomical Shoulder" Inverse/Reverse Humeral PE-Insert Sterile, Rx 2 11/06/2012 Zimmer, Inc.
Anatomical Shoulder" Inverse/Reverse Glenoid Sterile, Rx 2 11/06/2012 Zimmer, Inc.
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