Medical Device Recalls
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1 result found
510(K) Number: K251238 |
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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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| Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW HEMOPRO 3... | 2 | 09/25/2025 | Maquet Cardiovascular, LLC |
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