Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K023397 |
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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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ARCHITECT® Folate Low and Medium Controls, List 6C12-10; the kit contains 2 - 8 mL vials, Low Contro... | 3 | 07/20/2004 | Abbott Laboratories HPD/ADD/GPRD |
ARCHITECT Folate Specimen Diluent, List 6C12Y, 5.5 mL (100 tests) and 25.9 mL (500 tests) bottles co... | 3 | 07/20/2004 | Abbott Laboratories HPD/ADD/GPRD |
ARCHITECT Folate Manual Diluent, List 6C12-50; One 4 mL bottle of ARCHITECT Folate Manual Diluent co... | 3 | 07/20/2004 | Abbott Laboratories HPD/ADD/GPRD |
ARCHITECT Folate High Controls, List 6C12-11; the kit contains 8 - 1 mL vials of High Control H 15.0... | 3 | 07/20/2004 | Abbott Laboratories HPD/ADD/GPRD |
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