Maquet Cardiovascular, LLC: Medical Device Recall in 2023 - (Recall #: Z-1336-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System, Model Number C-VH-4000

Product Classification:

Class II

Date Initiated: March 6, 2023

Date Posted: April 12, 2023

Recall Number: Z-1336-2023

Event ID: 91764

Reason for Recall:

Some batches of product were not sterilized to their minimum sterilization specification.

Status: Ongoing

Product Quantity: 2300 units

Code Information:

UDI-DI: 00607567700406; Lot Numbers: 3000278401, 3000271148, 3000268643, 3000263026, 3000274504, 3000263925

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Brazil, China.

Voluntary or Mandated:

Voluntary: Firm initiated