Medical Device Recalls
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1 result found
Recall Number: Z-1072-2025 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| SenTiva, REF: 1000; SenTiva Duo, REF: 1000-D; Generators Part of the VNS Therapy System. Used for... | 2 | 01/31/2025 |
FEI # 1000117004 LivaNova USA, Inc. |
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