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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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Z-1330-2008 - Implantable Cardioverter Defibrillator
EPIC II VR Tiered-therapy cardioverter/defibrillator, Model V-158
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2
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08/19/2008
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St Jude Medical CRMD
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Z-1331-2008 - Implantable Cardioverter Defibrillator
EPIC II DR Tiered-therapy cardioverter/defibrillator, Model V-255
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2
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08/19/2008
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St Jude Medical CRMD
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Z-1332-2008 - Implantable Cardioverter Defibrillator
EPIC II+ DR Tiered-therapy cardioverter/defibrillator, Model V-258
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2
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08/19/2008
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St Jude Medical CRMD
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Z-1333-2008 - Implantable Cardioverter Defibrillator
EPIC II HF Tiered-therapy cardioverter/defibrillator with Biventricular Stimlation, Model V-355
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2
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08/19/2008
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St Jude Medical CRMD
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Z-1334-2008 - Implantable Cardioverter Defibrillator
EPIC II+ HF Tiered-therapy cardioverter/defibrillator with Biventricular Stimlation, Model V-357
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2
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08/19/2008
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St Jude Medical CRMD
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Z-1335-2008 - Implantable Cardioverter Defibrillator
EPIC II+ HF Tiered-therapy cardioverter/defibrillator with Biventricular Stimlation, Model V-356
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2
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08/19/2008
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St Jude Medical CRMD
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Z-1336-2008 - Implantable Cardioverter Defibrillator
ATLAS + VR Tiered-therapy cardioverter/defibrillator, Model V-193
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2
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08/19/2008
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St Jude Medical CRMD
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Z-1337-2008 - Implantable Cardioverter Defibrillator
ATLAS DR Tiered-therapy cardioverter/defibrillator, Model V-242
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2
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08/19/2008
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St Jude Medical CRMD
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Z-1338-2008 - Implantable Cardioverter Defibrillator
ATLAS + DR Tiered-therapy cardioverter/defibrillator, Model V-243
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2
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08/19/2008
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St Jude Medical CRMD
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Z-1339-2008 - Implantable Cardioverter Defibrillator
ATLAS + HF Tiered-therapy cardioverter/defibrillator with biventricular strimulation, Model V-341
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2
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08/19/2008
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St Jude Medical CRMD
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