Medical Device Recalls
-
11 to 15 of 15 Results
Recall Date to: 10/21/2014 PMA Number: P960009 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Medtronic DBS Lead Kit for Deep Brain Stimulation, 3389S-40, Medtronic, Inc. Minneapolis, MN 55432-5... | 2 | 06/15/2007 | Medtronic Neuromodulation |
Medtronic Activa PC, model 37601, and Activa RC, model 37612, Multi-program Rechargeable Neurostimul... | 2 | 10/31/2013 | Medtronic Neuromodulation |
Medtronic Activa PC, model 37601, and Activa RC, model 37612, Activa SC, models 37602 and 37603. Mu... | 2 | 11/14/2013 | Medtronic Neuromodulation |
Medtronic Activa Deep Brain Stimulation (DBS) system including the following system components: Mod... | 2 | 01/10/2006 | Medtronic Inc, Neurological & Spinal Division |
Medtronic Activa RC (37612), Activa PC (37601), Activa SC (37602), Activa SC (37603), Activa PC+S (... | 2 | 04/29/2014 | Medtronic Neuromodulation |
-