Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K063144 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| enGen(TM) Laboratory Automation Systems configured with Hettich Rotanta 46 RSC Robotic Centrifuges, ... | 2 | 01/26/2012 |
FEI # 1000136573 Ortho-Clinical Diagnostics |
| enGen Laboratory Automation System, Product Code engen, Software Versions enGen Select 3.2 and Above... | 3 | 07/08/2016 |
FEI # 1000136573 Ortho-Clinical Diagnostics |
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