Medical Device Recalls
-
1 to 4 of 4 Results
PMA Number: P980016/S114 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Medtronic Maximo II DR, model D284DRG. Digital dual chamber implantable cardioverter defibrillator ... | 2 | 10/21/2010 | Medtronic Inc. Cardiac Rhythm Disease Managment |
Medtronic Secura VR, model D224VRC, and model D234VRC not available in the U.S.. Digital single cha... | 2 | 10/21/2010 | Medtronic Inc. Cardiac Rhythm Disease Managment |
Medtronic Secura DR, model D224DRG, and model D234DRG not available in the U.S.. Digital Dual chamb... | 2 | 10/21/2010 | Medtronic Inc. Cardiac Rhythm Disease Managment |
Medtronic Maximo II VR, model D284VRC. Digital single chamber implantable cardioverter defibrillato... | 2 | 10/21/2010 | Medtronic Inc. Cardiac Rhythm Disease Managment |
-