Maquet Cardiovascular, LLC recalls VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500
- Recall date
- September 20, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0092-2025
- FDA classification
- Class I
- Brand / firm
- Maquet Cardiovascular, LLC
- Sold / distributed
- Worldwide distribution. US Nationwide. Brazil, China, and Hong Kong.
Why it was recalled
There were reports of the silicone detaching from the Jaws of the Harvesting Tool during use.
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500
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