Maquet Cardiovascular, LLC: Medical Device Recall in 2024 - (Recall #: Z-0723-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: December 1, 2023

Date Posted: January 24, 2024

Recall Number: Z-0723-2024

Event ID: 93615

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 554 units (OUS)

Code Information:

UDI-DI: 00607567700413, Lots: 3000283735, 3000293031, 3000310304, 3000333956.

Distribution Pattern:

US: OUS: China, Brazil, Hong Kong.

Voluntary or Mandated:

Voluntary: Firm initiated