Medical Device Recalls
-
|
1 result found
510(K) Number: K982132 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| AEROSET Immunoglobulin M, list number 1E01-01, manufactured by Abbott Laboratories, South Pasadena, ... | 2 | 07/20/2004 | Abbott Laboratories Diagnostic Div |
-







