|
Product Description
|
Recall Class
|
FDA Recall Posting Date
|
Recalling Firm
|
Z-1338-2008 - Implantable Cardioverter Defibrillator
ATLAS + DR Tiered-therapy cardioverter/defibrillator, Model V-243
|
2
|
08/19/2008
|
St Jude Medical CRMD
|
Z-1340-2008 - Implantable Cardioverter Defibrillator
ATLAS + HF Tiered-therapy cardioverter/defibrillator with biventricular stimulation, Model V-340
|
2
|
08/19/2008
|
St Jude Medical CRMD
|
Z-1341-2008 - Implantable Cardioverter Defibrillator
ATLAS + HF Tiered-therapy cardioverter/defibrillator with biventricular stimulation, Model V-343
|
2
|
08/19/2008
|
St Jude Medical CRMD
|
Z-1339-2008 - Implantable Cardioverter Defibrillator
ATLAS + HF Tiered-therapy cardioverter/defibrillator with biventricular strimulation, Model V-341
|
2
|
08/19/2008
|
St Jude Medical CRMD
|
Z-1336-2008 - Implantable Cardioverter Defibrillator
ATLAS + VR Tiered-therapy cardioverter/defibrillator, Model V-193
|
2
|
08/19/2008
|
St Jude Medical CRMD
|
Z-1337-2008 - Implantable Cardioverter Defibrillator
ATLAS DR Tiered-therapy cardioverter/defibrillator, Model V-242
|
2
|
08/19/2008
|
St Jude Medical CRMD
|
Z-1343-2008 - Implantable Cardioverter Defibrillator
ATLAS II DR Tiered-therapy cardioverter/defibrillator, Model V-265
|
2
|
08/19/2008
|
St Jude Medical CRMD
|
Z-1345-2008 - Implantable Cardioverter Defibrillator
ATLAS II HF Tiered-therapy cardioverter/defibrillator with biventricular stimulation, Model V-365
|
2
|
08/19/2008
|
St Jude Medical CRMD
|
Z-1342-2008 - Implantable Cardioverter Defibrillator
ATLAS II VR Tiered-therapy cardioverter/defibrillator, Model V-168
|
2
|
08/19/2008
|
St Jude Medical CRMD
|
Z-1344-2008 - Implantable Cardioverter Defibrillator
ATLAS II+ DR Tiered-therapy cardioverter/defibrillator, Model V-268
|
2
|
08/19/2008
|
St Jude Medical CRMD
|