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® 4600 Chemistry System, Product Code: 6802445 Product Usage: Fo... | 2 | 04/26/2012 |
FEI # 1000305841 Ortho-Clinical Diagnostics |
| 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 |
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