Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K111387 |
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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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cobas LiatSystem, respiratory virus panel nucleic acid assay system, Material Number 07341920190 | 2 | 03/28/2022 | Roche Molecular Systems, Inc. |
cobas® Liat® Analyzer | 2 | 07/15/2016 | Roche Molecular Systems, Inc. |
cobas® Liat Influenza A/B Quality Control Kit; For use with cobas® Liat Influenza A/B Assay. | 3 | 07/13/2016 | Roche Molecular Systems, Inc. |
cobas Liat Analyzer, for in vitro diagnostic use. | 2 | 09/02/2015 | Roche Molecular Systems, Inc. |
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