Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Z-2750-2026 - FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percutaneous Cardiac Ablation Catheter | 2 | 07/17/2026 |
FEI # 2124215 Boston Scientific Corporation |
| Z-2752-2026 - FARASTAR PFA Generator, Product ID M004PFCE61M460; Percutaneous Cardiac Ablation Catheter | 2 | 07/17/2026 |
FEI # 2124215 Boston Scientific Corporation |
| Z-2751-2026 - FARASTAR Pulsed Field Ablation Generator, Product ID M004PFCE61M401; Percutaneous Cardiac Ablation Catheter | 2 | 07/17/2026 |
FEI # 2124215 Boston Scientific Corporation |
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