Medical Device Recalls
-
1 result found
Recall Date to: 09/01/2014 PMA Number: P990001 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Vitatron C-Series C60DR DDDR Dual Chamber Rate Responsive Pacemaker includes the following models: C... | 2 | 07/07/2007 | Medtronic Inc. Cardiac Rhythm Managment |
-