Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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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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| Z-0726-2026 - Aurora EV-ICD and Clinical EV-ICD, single chamber, extravascular implantable cardioverter defibrillators (ICD), Product Number DVEA3E4 | 2 | 11/28/2025 | Medtronic, Inc. |
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