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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
Related Medical Device Recalls Date Classified to: 08/30/2014
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Product Description
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Recall
Class
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Date
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Recalling Firm
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Z-0700-2008 - Biomet RINGLOC + Instrumentation Impactor Plate, Size 20; REF/Part #: 31-400620, Biomet Orthopedics, Inc., Warsaw, IN. 2 Feb-05-2008 Biomet, Inc.
Z-0701-2008 - Biomet RINGLOC + Instrumentation Impactor Plate, Size 21; REF 31-400621,Biomet Orthopedics, Inc., Warsaw, IN. 2 Feb-05-2008 Biomet, Inc.
Z-0705-2008 - Biomet RINGLOC + Instrumentation Impactor Plate, Size 28; REF/Part#: 31-400628, Biomet Orthopedics, Inc., Warsaw, IN. 2 Feb-05-2008 Biomet, Inc.
Z-0703-2008 - Biomet RINGLOC + Instrumentation Impactor Plate, Size 23; REF/Part#: 31-400623, Biomet Orthopedics, Inc., Warsaw, IN. 2 Feb-05-2008 Biomet, Inc.
Z-0704-2008 - Biomet RINGLOC + Instrumentation Impactor Plate, Size 26; REF/Part#: 31-400626, Biomet Orthopedics, Inc., Warsaw, IN. 2 Feb-05-2008 Biomet, Inc.
Z-0702-2008 - Biomet RINGLOC + Instrumentation Impactor Plate, Size 22; REF/Part#: 31-400622, Biomet Orthopedics, Inc., Warsaw, IN. 2 Feb-05-2008 Biomet, Inc.
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