Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K031924 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| VITROS® 5,1 FS (Fusion Series) Chemistry System Software Version 2.2.1, only when using VITROS® Chem... | 2 | 08/16/2007 |
FEI # 1000136573 Ortho-Clinical Diagnostics |
| VITROS Software Version 3.1 utilized on the following systems: 1) 4600 Chemistry Systems (VITROS 5,1... | 3 | 01/20/2015 |
FEI # 1000136573 Ortho-Clinical Diagnostics |
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