Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0594-2013 - Zimmer Spine Ardis Inserter, Rx, non-sterile | 1 | 12/22/2012 |
FEI # 1000220733 Zimmer, Inc. |
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