Medical Device Recalls
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1 to 2 of 2 Results
PMA Number: P010031/S084 |
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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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Medtronic Consulta CRT-D, model D224TRK and Model D234TRK not available in the US. Digital implant... | 2 | 10/21/2010 | Medtronic Inc. Cardiac Rhythm Disease Managment |
Medtronic Maximo II CRT-D, model D284TRK. Digital implantable cardioverter defibrillator with cardi... | 2 | 10/21/2010 | Medtronic Inc. Cardiac Rhythm Disease Managment |
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