Maquet Cardiovascular, LLC: Medical Device Recall in 2025 - (Recall #: Z-0711-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

VasoView HemoPro 2 Endoscopic Vessel Harvesting System. Model Numbers: VH-4000. Indicated for use in minimally invasive surgery allowing access for vessel harvesting.

Product Classification:

Class I

Date Initiated: December 9, 2024

Date Posted: January 15, 2025

Recall Number: Z-0711-2025

Event ID: 95908

Reason for Recall:

Potential for two issues: 1. Bent or detached heater wire; 2. Silicone peeling or detaching from the Jaws of the Harvesting Tool

Status: Ongoing

Product Quantity: 418,076 units (326,608 US, 91,468 OUS)

Code Information:

Model Number: VH-4000. UDI-DI: 00607567700406. All unexpired Lots.

Distribution Pattern:

Nationwide distribution. International distribution to Australia, Austria, Bahrain, Bangladesh, Belgium, Canada, Czech Republic, Denmark, Finland, France, Germany, Guatemala, Hong Kong, India, Iran, Iraq, Ireland, Italy, Japan, Jordan, Kenya, Kuwait, Malaysia, Mexico, Netherlands, Netherlands, New Zealand, Oman, Panama, Puerto Rico, Philippines, Poland, Portugal, Qatar, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, Turkey, United Arab Emirates.

Voluntary or Mandated:

Voluntary: Firm initiated