Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Z-1650-2021 - Cobalt HF Quad MRI SureScan Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D) - Product Usage: are multiprogrammable cardiac devices that monitor and regulate a pa... | 2 | 05/20/2021 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
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