Medical Device Recalls
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1 result found
PMA Number: P240006 |
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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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| VARIPULSE Bi-Directional Ablation Catheter REF D141201. The Field Catheter is indicated for us... | 1 | 02/28/2025 |
FEI # 3013300026 Biosense Webster, Inc. |
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