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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: K111188
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Product Description
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FDA Recall
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Cobas b 123 POC system cobas b 123 POC system is fully automated POC system for whole blood in vi... 2 12/13/2012 Roche Diagnostics Operations, Inc.
cobas b 123 Fluid Pack COOX REF 05169992001 200 Product Usage: The cobas b 123 POC system is a f... 2 08/21/2015 Roche Diagnostics Operations, Inc.
cobas b 123 Fluid Pack COOX REF 05170036001 400 Product Usage: The cobas b 123 POC system is a f... 2 08/21/2015 Roche Diagnostics Operations, Inc.
Cobas b 123 POC system The cobas b 123 POC system is a fully automated POC system for whole blood i... 2 01/23/2017 Roche Diagnostics Operations, Inc.
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