Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K924396 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Factor deficient plasma for the Siemens BCS® / BCS® XP System. In vitro diagnostic reagent for th... | 2 | 06/05/2015 | Siemens Healthcare Diagnostics, Inc. |
| Coagulation Factor VIII Deficient Plasma (OTXW). Factor Deficiency Test | 3 | 08/16/2005 | Dade Behring , Inc. |
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