FDADecember 1, 2023device

Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W .

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

maquet cardiovascularmaquet

UPCs

00607567700413

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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