Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vasoview Hemopro Endoscopic Vessel Harvesting System Recalled by Maquet Cardiovascular, LLC Due to Risk of polyimide particulate matter being present on...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Maquet Cardiovascular, LLC directly.
Affected Products
Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W .
Quantity: 554 units (OUS)
Why Was This Recalled?
Risk of polyimide particulate matter being present on the endoscopic harvesting vessel system. This issue may result in polyimide particulate matter being introduced into the arterial conduit for patients undergoing a coronary artery bypass graft (CABG) or peripheral bypass graft surgery.
Where Was This Sold?
US: OUS: China, Brazil, Hong Kong.
About Maquet Cardiovascular, LLC
Maquet Cardiovascular, LLC has 251 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report