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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls Recall Date to: 09/02/2015
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Product Description
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FDA Recall
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Recalling Firm
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Z-1690-2008 - Universal Notch Preparation Guide, Size #3; Non Sterile; Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430; authorized representative in Europe: Stryker France ZAC Satolas Green Pus... 2 09/20/2008 Stryker Howmedica Osteonics Corp.
Z-1691-2008 - X-Celerate Universal Block Pegless Size #3, Non Sterile; 2 09/20/2008 Stryker Howmedica Osteonics Corp.
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