Medical Device Recalls
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1 result found
Recall Number: Z-2638-2025 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to identify internal wiring an... | 2 | 09/26/2025 |
FEI # 2020394 Bard Peripheral Vascular Inc |
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