Medical Device Recalls
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1 to 2 of 2 Results
PMA Number: P890003/S386 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CRT-P Quad Models (CRT-Ps): a. Percepta CRT-P MRI: W1TR01, W1TR04, W4TR01, W4TR04 b. Serena CRT-P... | 2 | 04/30/2021 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| CareLink SmartSync Device Manager (24970A). used to interrogate cardiac implantable electronic devi... | 2 | 04/30/2021 |
FEI # 2182208 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
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