Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K071041 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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CoaguChek XS Plus System The CoaguChek XS Plus system for use by professional healthcare provider... | 2 | 06/24/2013 | Roche Diagnostics Operations, Inc. |
Roche CoaguChek XS System, CoaguChek XS Plus Care Kit, Roche Diagnostics, Indianapolis, IN; Model Nu... | 2 | 09/03/2009 | Roche Diagnostics Operations, inc. |
CoaguChek® XS System Prothrombin time test: CoaguChek XS PT Test 2X24 Strips, Catalog Number: 04625... | 1 | 11/02/2018 | Roche Diagnostics Corporation |
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