Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K062925 |
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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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Roche Coaguchex XS Systems for Patient Self-Testing, Roche Diagnostics, Indianapolis, IN; REF 048377... | 2 | 08/11/2009 | Roche Diagnostics Corp. |
Roche CoaguChek XS System, CoaguChek XS PST Kit, Roche Diagnostics, Indianapolis, IN; Catalog/Model ... | 2 | 09/03/2009 | Roche Diagnostics Operations, inc. |
CoaguChek XS System (PST) The CoaguChek XS PT test strips are part of the CoaguChek XS System. Th... | 2 | 06/24/2013 | Roche Diagnostics Operations, Inc. |
CoaguChek XS PST Meters- IVD (Patient Self-Testing) measures blood-clotting time for people who are ... | 2 | 01/07/2021 | Roche Diagnostics Operations, Inc. |
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