Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K983759 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ARCHITECT Ferritin Reagent; in vitro diagnostic; list numbers 6C11-20 (4 x 100 tests), 6C11-25 (1 x ... | 3 | 07/04/2006 | Abbott Laboratories MPG |
| Alinity i Ferritin Reagent Kit, List Number 07P6530 The Alinity i Ferritin assay is a chemilumin... | 2 | 08/07/2019 | Abbott Ireland Diagnostics Division |
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