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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-1320-2008 - Implantable Cardioverter Defibrillator
EPIC VR Tiered-therapy Cardioverter/Defibrillator, Model V-197
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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-1347-2008 - Implantable Cardioverter Defibrillator
ATLAS II+ HF Tiered-therapy cardioverter/defibrillator with biventricular stimulation, Model V-367
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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-1322-2008 - Implantable Cardioverter Defibrillator
EPIC HF Tiered-therapy cardioverter/defibrillator with biventricular stimulation, Model V-337
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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-1323-2008 - Implantable Cardioverter Defibrillator
EPIC HF Tiered-Therapy Cardioverter/Defibrillator with Biventricular Stimulation, Model V-338
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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-1324-2008 - Implantable Cardioverter Defibrillator
EPIC HF Tiered-therapy Cardioverter/defibrillator with biventricular stimulation, Model V-339
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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-1325-2008 - Implantable Cardioverter Defibrillator
EPIC + VR Tiered-therapy cardioverter/defibrillator, Model V-196
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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-1326-2008 - Implantable Cardioverter Defibrillator
EPIC DR Tiered-therapy cardioverter/defibrillator, Model V-233
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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-1327-2008 - Implantable Cardioverter Defibrillator
EPIC + DR Tiered-therapy cardioverter/defibrillator, Model V-236
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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-1328-2008 - Implantable Cardioverter Defibrillator
EPIC + DR Tiered-therapy cardioverter/defibrillator, Model V-239
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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-1329-2008 - Implantable Cardioverter Defibrillator
EPIC + HF Tiered-therapy cardioverter/defibrillator with biventricular stimulation, Model V-350
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2
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08/19/2008
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St Jude Medical CRMD
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