Medical Device Recalls
-
31 to 31 of 31 Results
Recall Date to: 08/01/2014 PMA Number: P010012 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Guidant, CONTAK RENEWAL 3/3RF Models H170, H175, H177, H179, H210, H215, H217, H219, Guidant Corpor... | 2 | 10/07/2010 | Boston Scientific CRM Corp |
-