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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K862140
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Product Description
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Recall
Class
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FDA Recall
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MicroScan -Neg Breakpoint Combo Panel Type 34; Catalog number B1017-404; Panel MicroScan Neg Break... 2 04/26/2015 Beckman Coulter, Inc.
MicroScan Dried Overnight Gram Negative Panels; Panel type: Neg Breakpoint Combo Type 47, catalog... 2 05/08/2012 Siemens Healthcare Diagnostics, Inc.
MicroScan Dried Overnight Gram Negative Panels; Panel type: Neg Urine Combo 55; Catalog Number B1... 2 05/08/2012 Siemens Healthcare Diagnostics, Inc.
MicroScan Dried Overnight Gram Negative Panels; Panel type: Neg Breakpoint Combo Type 34, catalog... 2 05/08/2012 Siemens Healthcare Diagnostics, Inc.
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