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Maquet Cardiovascular, LLC recalls Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W .
Recalled January 24, 2024 · FDA recall Z-0723-2024 · Maquet Cardiovascular
Hazard
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. · FDA Class II
Units
554 units (OUS)
Sold at
US: OUS: China, Brazil, Hong Kong.
Description
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.
Product
Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W .
Manufacturer(s)
Maquet Cardiovascular, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →