Maquet Cardiovascular, LLC: Medical Device Recalls in 2023
Updated on March 25, 2026.
According to to data from the FDA, there were 13 medical device recalls made by Maquet Cardiovascular, LLC in 2023. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Model Number C-VH-3500
- VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System, Model Number C-VH-4000
- VASOVIEW HEMOPRO, OUS, Endoscopic Vessel Harvesting System, Model Number C-VH-3000-W
- Vasoshield Syringe Packs, Model VH-5001
- Hemopro 2 with Vasoshield, Model VH-4001
- Fusion Bioline Vascular Graft, Part number M00201503046B0
- Maquet Acrobat-i Vacuum Stabilizer System Intended for use during performance of cardiac surgical procedures through a sternotomy incision approach. Product Code: OM-10000Z
- ACROBAT-i Vacuum Stabilizer System, Part Number C-OM-10000. Component of a chest stabilization system for cardiac and chest surgery.
- ACROBAT SUV Vacuum Off-Pump System, Part Number C-OM-9000S. Component of a chest stabilization system for cardiac and chest surgery.
- ACROBAT V Vacuum Off-Pump System, Part Number C-OM-9100S. Component of a chest stabilization system for cardiac and chest surgery.
- Acrobat-i Vacuum Positioner System, Model Number XP-5000Z
- Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, outer box artwork for Vasoview Hemopro 2 (HP2).
- ACCESSRAIL Platform (Standard Blade) Part Number SB-1000, and (Deep Blades) Part Number C-DB-1000. Component of a chest stabilization system for cardiac and chest surgery.