Medical Device Recalls
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1 to 5 of 5 Results
PMA Number: P010031/S513 |
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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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Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), Amplia MRI. Labeled as the following: ... | 1 | 02/01/2018 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), Compia MRI. Labeled as the following: ... | 1 | 02/01/2018 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), Claria MRI. Labeled as the following: ... | 1 | 02/01/2018 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
Amplia MRI Quad CRT-0 SureScan Claria MRI Quad CRT-D SureScan Compia MRI Quad CRT-D SureScan | 2 | 05/19/2017 | Medtronic Inc., Cardiac Rhythm and Heart Failure |
Amplia MRI" CRT -D SureScan", Amplia MRI" Quad CRT -D SureScan", Claria MRI" CRT -D SureScan", ... | 2 | 01/07/2017 | Medtronic Inc., Cardiac Rhythm and Heart Failure |
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