Medical Device Recalls
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1 to 3 of 3 Results
PMA Number: P950022 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Optisure Dual Coil Defibrillation Leads, Model No. LDA220, LDA220Q, LDA230Q, LDP220Q. St. Jude Medi... | 1 | 01/21/2016 | St Jude Medical Cardiac Rhythm Management Division |
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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