Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K954045 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
AxSYM Rubella IgG Reagent Pack; Abbott Laboratories, Abbott Park, IL 60064; list 3B23-20 The AxS... | 3 | 09/16/2008 | Abbott Laboratories |
AxSYM Rubella IgG Reagent Pack; list 03B23; 100 test pack; an in vitro diagnostic; Abbott Laboratori... | 2 | 07/11/2007 | Abbott Laboratories |
-