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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
Recall Date to: 12/18/2014 PMA Number: P950022
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Product Description
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FDA Recall
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St. Jude Medical Riata ST Silicone Endocardial Defibrillation Leads Riata(7Fr), Models: 7000, 7001, ... 1 01/11/2012 St Jude Medical CRMD
St. Jude Medical Riata (8Fr), Models: 1560, 1561, 1562, 1570, 1571, 1572, 1580, 1581, 1582, 1590, 15... 1 01/11/2012 St Jude Medical CRMD
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