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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Product Description
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Z-0321-2012 - Zimmer ZMR Hip System Instructions for Use, utilized for the following ZMR devices: Porous Stem,Nitrited Porous Revision, Slotted Porous Bowed Stems with and without Compression Nut, Splined Straight ... 2 12/01/2011 FEI # 1000220733
Zimmer Inc.
Z-0324-2012 - ZMR Over the Junction Instruments for Revision, utilized for the following ZMR devices: Porous Stem,Nitrited Porous Revision, Slotted Porous Bowed Stems with and without Compression Nut, Splined Strai... 2 12/01/2011 FEI # 1000220733
Zimmer Inc.
Z-0323-2012 - ZMR Crossover Instrumentation, utilized for the following ZMR devices: Porous Stem,Nitrited Porous Revision, Slotted Porous Bowed Stems with and without Compression Nut, Splined Straight Stem, Taper S... 2 12/01/2011 FEI # 1000220733
Zimmer Inc.
Z-0322-2012 - ZMR Porous Revision Hip Prosthesis Surgical Technique, utilized for the following ZMR devices: Porous Stem,Nitrited Porous Revision, Slotted Porous Bowed Stems with and without Compression Nut, Spline... 2 12/01/2011 FEI # 1000220733
Zimmer Inc.
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