Medical Device Recalls
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151 to 160 of 301 Results
Product: pacemaker |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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|---|---|---|---|
| ESSENTIO MRI DR Pacemaker | 2 | 01/15/2018 | Boston Scientific Corporation |
| ESSENTIO EL DR Pacemaker | 2 | 01/15/2018 | Boston Scientific Corporation |
| ESSENTIO MRI EL DR Pacemaker | 2 | 01/15/2018 | Boston Scientific Corporation |
| PROPONENT SR Pacemaker | 2 | 01/15/2018 | Boston Scientific Corporation |
| PROPONENT DR Pacemaker | 2 | 01/15/2018 | Boston Scientific Corporation |
| PROPONENT EL DR Pacemaker | 2 | 01/15/2018 | Boston Scientific Corporation |
| PROPONENT VDD SL Pacemaker | 2 | 01/15/2018 | Boston Scientific Corporation |
| PROPONENT MRI Pacemaker | 2 | 01/15/2018 | Boston Scientific Corporation |
| Azurion 3 M12, Azurion 3 M15, Allura R9 7 M12, Allura R9 M20, Azurion 7 M12, Azurion 7 M20 The ... | 2 | 12/18/2017 | Philips Electronics North America Corporation |
| Regard, Item Number: 880328002, Sterile, HT0759B - Pacemaker Pk - OSU | 2 | 03/24/2017 | Resource Optimization & Innovation Llc |
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