Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K001981 |
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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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DiaSorin Anti-Cardiolipin IgA ELISA Kit, catalog no. 7800. Manufactured for: DiaSorin Inc. 1951 No... | 3 | 06/25/2005 | Diasorin Inc. |
DiaSorin Anti-Cardiolipin IgA ELISA kit for the detection in human serum or plasma of antoantibodies... | 2 | 03/18/2005 | Diasorin Inc. |
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