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U.S. Department of Health and Human Services

Medical Device Recalls

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41 to 44 of 44 Results
Related Medical Device Recalls Recall Date to: 07/28/2015
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Product Description
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FDA Recall
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Z-1005-2014 - VERSA-FX II KEYLESS TUBE, VERSA-FX II KEYLESS SHORT, VERSA-FX II SHORT TUBE PL, VERSA-FX II STD TUBE PLAT and VERSA-FX II SUPRACONDYLR Item codes starting with 0011930, 0011931 and 0011941 2 02/20/2014 Zimmer, Inc.
Z-1006-2014 - VERSA-FX KEYLESS 90D X 8 and X 11, VERSA-FX KEYLESS 95D X 8, X 11, and X 14, VERSA-FX KEYLESS 140D X 4 and X 5, VERSA-FX KEYLESS 135D X 4 and X 5, VERSA-FX SHORT TUBE, 130D, 135D and 140D, VERSA-FX ST... 2 02/20/2014 Zimmer, Inc.
Z-1028-2014 - VERSYS HERITAGE FEM STEM 2 02/20/2014 Zimmer, Inc.
Z-1030-2014 - ZIMTRON 6 DEG 22 HEADS 2 02/20/2014 Zimmer, Inc.
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