Device recall: The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use Class II device that was cleared for marketing by FDA under 510(k) number K101274.
Official structured record identifier: 99259.
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USA
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- Publisher
- openFDA Device Recalls
- Region
- USA
- Scope
- Regulatory
- Published
- July 22, 2026
- Language
- EN
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Official structured record identifier: 99259.
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Source: openFDA Device Recalls
Scope: Regulatory
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