Maquet Cardiovascular, LLC: Medical Device Recall in 2025 - (Recall #: Z-2636-2025)

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 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW HEMOPRO 3 Endoscopic Vessel Harvesting (EVH) System (VH-6000, VH-6001, and VH-6010) is a vessel harvesting kit designed for use with a 7 mm endoscope to cut and cauterize vessel branches. The HP3 Harvesting Tool features two curved, insulated jaws with heating elements that operate through heat and pressure rather than radiofrequency energy.

Product Classification:

Class II

Date Initiated: August 6, 2025
Date Posted: October 1, 2025
Recall Number: Z-2636-2025
Event ID: 97469
Reason for Recall:

Reports of out-of-box failures discovered during the limited launch phase. Failure modes included angled deformity at the attachment site of the Harvesting Tool Jaws and the distal end of the Harvesting Tool Shaft, jaws not fully closed out of box, and heater wire lifted/flexed away from jaws.

Status: Ongoing
Product Quantity: 98 units
Code Information:

Model No. C-VH-6000; UDI: 00607567701274; Lot/Serial No. 3000486429, 3000487231, 3000487726, 3000488639.

Distribution Pattern:

US Nationwide distribution in the states of FL, IL, MD & TX.

Voluntary or Mandated:

Voluntary: Firm initiated