Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K963926 |
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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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CA 15-3 Controls, list 9C08-10; an In Vitro diagnostic for use with the AxSYM or IMx CA 15-3 reagent... | 3 | 07/18/2006 | Abbott Laboratories MPG |
CA 15-3 Calibrators, list 9C08-01; the pack contains six 4-mL bottles of 115D8:DF3 reactive determin... | 2 | 03/26/2003 | Abbott Laboratories HPD/ADD |
AxSYM CA 15-3 Reagent Pack; list 03B42; 100 test pack; an in vitro diagnostic; Abbott Laboratories, ... | 2 | 07/11/2007 | Abbott Laboratories |
Abbott AxSYM CA 15-3 Master Calibrator Pack, list 3B42-30; the pack contains two 4-mL bottles, with ... | 2 | 03/26/2003 | Abbott Laboratories HPD/ADD |
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