Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K984108 |
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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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B12 Reagent (6C09-20 and 6C09-25) for use with the ARCHITECT i2000 and i2000SR Analyzers, List numbe... | 2 | 01/26/2005 | Abbott Laboratories, Inc |
ARCHITECT B12 Reagents, List 6C09-20 (4 x 100 tests) and List 6C09-25 (100 tests); Abbott Laboratori... | 3 | 09/14/2004 | Abbott Laboratories HPD/ADD/GPRD |
ARCHITECT B12 Reagent, list 06C09-22 (4 x 100 tests), 06C09-27 (1 x 100 tests); an in vitro diagnost... | 3 | 05/11/2006 | Abbott Laboratories MPG |
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