Class I

Medical Device Recall: VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500

Maquet Cardiovascular, LLC · September 20, 2024

Reason for Recall

There were reports of the silicone detaching from the Jaws of the Harvesting Tool during use.

Distribution

Worldwide distribution. US Nationwide. Brazil, China, and Hong Kong.

States Affected

NATIONWIDE

Quantity Affected

28,809 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0092-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.