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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls Recall Date to: 12/19/2014
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Product Description
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Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-0319-2008 - Biomet Optigun Cement Gun, Ratchet, non-sterile; REF 419500 and REF 4195 (in Europe), Biomet, Inc., Warsaw, IN 2 12/22/2007 Biomet, Inc.
Z-0318-2008 - Biomet Optigun Cement Gun, non-sterile; REF 419300 and REF 4193 (in Europe), Biomet, Inc., Warsaw, IN 2 12/22/2007 Biomet, Inc.
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