Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K112343 |
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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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Centaur Syphilis Assay-SYP Kit, 200 Test - Product Usage: For in vitro diagnostic use in the qualita... | 2 | 05/24/2021 | Siemens Healthcare Diagnostics, Inc |
Siemens ADVIA Centaur® Syphilis (SYPH) Assay , 200 ReadyPack Reference Number 10492493 Product... | 2 | 08/20/2012 | Siemens Healthcare Diagnostics, Inc |
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