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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K060256
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Unicel DxC 600i System and Unicel Dxl 600 Access Immunoassay System 2 09/21/2008 FEI # 2050012
Beckman Coulter Inc
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