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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 34 of 34 Results
Recall Date to: 04/21/2014 PMA Number: P910023
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Product Description
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FDA Recall
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Implantable Cardioverter Defibrillator EPIC VR Tiered-therapy Cardioverter/Defibrillator, Model V-... 2 08/19/2008 St Jude Medical CRMD
Implantable Cardioverter-Defibrillator Models affected include the following: Atlas+ Models V-... 2 04/13/2005 St Jude Medical
Photo DR, Model V-230HV Implantable Cardioverter Defibrillator 2 11/16/2005 St Jude Medical
Photo Micro VR/DR Models V-194 2 11/16/2005 St Jude Medical
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