Maquet Cardiovascular, LLC
252 recalls on record · Latest: Jul 22, 2026
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Agency notice ledger
Federal filing book Maquet Cardiovascular, LLC HEAVY-BOOK · SINGLE-AGENCY
#52 of 14,151 · 252 notices · 0.241% archive
- BOOK 252 notices
- RANK #52 of 14,151
- SHARE 0.241% archive
- AGENCY FDA Devices (252)
- CAT medical devices
- CATS 1 category
- LATEST Jul 22, 2026
- PHOTO Nissan
Nearest notice-volume peer: Nissan (1 notice gap)
Maquet Cardiovascular, LLC accounts for about 0.241% of the 104,423-notice archive on 252 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →
Maquet Cardiovascular, LLC's standing among 14,151 recalling firms
Maquet Cardiovascular, LLC ranks 52nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
Maquet Cardiovascular, LLC vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
252 52nd of 14151 higher than 14,099 of 14,151 firms
Firms, banded by distinct federal recall-event inventory
Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13
Maquet Cardiovascular, LLC in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
- Hospira Inc.
Hospira Inc.
257 notices
- Intuitive Sur…
Intuitive Surgical, Inc.
257 notices
- Biomet, Inc.
Biomet, Inc.
255 notices
- Nissan
Nissan
253 notices
- Maquet Cardio… (this)
Maquet Cardiovascular, LLC
252 notices
- Volvo
Volvo
248 notices
What this shows Maquet Cardiovascular, LLC holds about 0.241% of archive notices alongside 252 distinct filings.
FDA Devices Moderate Jul 22, 2026
The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use Class II device that was cleared for marketing by FDA under 510(k) number K101274.
FDA Devices Moderate Oct 1, 2025
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.
FDA Devices Moderate Sep 24, 2025
Heartstring III Proximal Seal System. Intravascular anastomosis occluder.
FDA Devices Moderate Sep 24, 2025
Heartstring III Proximal Seal System, 3.8 MM. Intravascular anastomosis occluder.
FDA Devices Moderate Sep 24, 2025
Heartstring III Proximal Seal System, 4.3 MM. Intravascular anastomosis occluder.
FDA Devices Moderate Apr 30, 2025
The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed for use in conjunction with the 7 mm extended length endoscope. The Harvesting Cannula has four lumens which house the endoscope, C-Ring, distal lens washer tube, and Harvesting Tool for cutting and cauterizing vessel branches. The Harvesting Tool has two curved jaws. One of the jaws contains the heating elements for branch cutting and cauterization and spot cautery. An area near the tip of the convex side of the jaw is used
FDA Devices Moderate Apr 23, 2025
Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro 2).
FDA Devices Critical Jan 15, 2025
VasoView HemoPro 2 Endoscopic Vessel Harvesting System. Model Numbers: VH-4000. Indicated for use in minimally invasive surgery allowing access for vessel harvesting.
FDA Devices Critical Jan 15, 2025
Vasoview Hemopro 2 (w/Vasoshield) Endoscopic Vessel Harvesting System. Model Numbers: VH-4001. Indicated for use in minimally invasive surgery allowing access for vessel harvesting.
FDA Devices Moderate Nov 27, 2024
Acrobat-i Vacuum Stabilizer System. Model Number C-OM-10000Z
FDA Devices Moderate Nov 27, 2024
Acrobat SUV Vacuum Stabilizer System, ST. Model Number C-OM-9000Z
FDA Devices Moderate Nov 27, 2024
Acrobat-i Positioner. Model Number C-XP-5000Z
FDA Devices Critical Nov 6, 2024
VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500
FDA Devices Moderate Jul 17, 2024
The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens washer tube, and harvesting tool for cutting and cauterizing vessel branches. The harvesting tool has two curved jaws. One of the jaws contains the heating elements for branch cutting and cauterization and spot cautery. An area near the tip of the convex side of the jaw is us
FDA Devices Moderate Jul 17, 2024
The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens washer tube, and harvesting tool for cutting and cauterizing vessel branches. The harvesting tool has two curved jaws. One of the jaws contains the heating elements for branch cutting and cauterization and spot cautery. An area near the tip of the convex side of the jaw is use
FDA Devices Moderate Jul 3, 2024
The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System, labeled as the following: 1. VasoView Hemopro 2, Model Number: VH-4000. 2. VasoView Hemopro 2 with Vasoshield. Model Number: VH-4001. The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting Systems are designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens washer tube, and harvesting tool for cutting and cauterizing vessel branches. Th
FDA Devices Moderate Jul 3, 2024
The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens washer tube, and harvesting tool for cutting and cauterizing vessel branches. The harvesting tool has two curved jaws. One of the jaws contains the heating elements for branch cutting and cauterization and spot cautery. An area near the tip of the convex side of the jaw is use
FDA Devices Moderate Jan 24, 2024
Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W .
FDA Devices Critical Jan 24, 2024
Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit
FDA Devices Critical Jan 24, 2024
Product REF 4000-100N, DRAIN, EXPRESS SINGLE W/AC, Single Collection
FDA Devices Moderate Jan 24, 2024
Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3500.
FDA Devices Moderate Dec 27, 2023
Acrobat-i Vacuum Positioner System, Model Number XP-5000Z
FDA Devices Moderate Nov 8, 2023
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).
FDA Devices Moderate Nov 1, 2023
Maquet Acrobat-i Vacuum Stabilizer System Intended for use during performance of cardiac surgical procedures through a sternotomy incision approach. Product Code: OM-10000Z
FDA Devices Moderate Aug 9, 2023
ACROBAT SUV Vacuum Off-Pump System, Part Number C-OM-9000S. Component of a chest stabilization system for cardiac and chest surgery.
FDA Devices Moderate Aug 9, 2023
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.
FDA Devices Moderate Aug 9, 2023
ACROBAT-i Vacuum Stabilizer System, Part Number C-OM-10000. Component of a chest stabilization system for cardiac and chest surgery.
FDA Devices Moderate Aug 9, 2023
ACROBAT V Vacuum Off-Pump System, Part Number C-OM-9100S. Component of a chest stabilization system for cardiac and chest surgery.
FDA Devices Moderate Apr 12, 2023
VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System, Model Number C-VH-4000
FDA Devices Moderate Apr 12, 2023
VASOVIEW HEMOPRO, OUS, Endoscopic Vessel Harvesting System, Model Number C-VH-3000-W
FDA Devices Moderate Apr 12, 2023
VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Model Number C-VH-3500
FDA Devices Moderate Mar 22, 2023
Fusion Bioline Vascular Graft, Part number M00201503046B0
FDA Devices Moderate Jan 25, 2023
Vasoshield Syringe Packs, Model VH-5001
FDA Devices Moderate Jan 25, 2023
Hemopro 2 with Vasoshield, Model VH-4001
FDA Devices Moderate Jun 29, 2022
INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour surface and non-velour inner surface. The device is available in straight tubes and bifurcated configurations, as well as hemabridge, aortic arch, thoracic aortic graft, and cardioroot configurations designed for use on the thoracic aorta
FDA Devices Moderate Apr 13, 2022
Ultima Activator II Reusable Drive Mechanism, part # C-UA-5001. Labeled REF UA-5001.
FDA Devices Moderate Mar 16, 2022
HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. Product Code/REF Number: M002020952070
FDA Devices Moderate Dec 29, 2021
Hemashield Gold Knitted Bifurcated, 18 mm x 9 mm; reference number M002020851890
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch, Product Code: M00202175912P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175930P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M00202175826P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175822P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
Hemashield Gold Knitted Microvel Double Velour Vascular Graft Axillo-bifemoral, Product Code: M002020955890 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch, Product Code: M00202175730AP0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft01 Branch, Product Code: M00202175834P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M00202175832P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175732P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175924P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Thoracoabdominal, Product Code: M00202175428T0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
FDA Devices Moderate May 13, 2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch, Product Code: M00202175928P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Maquet Cardiovascular, LLC carries an outsized archive share
Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.
Similar recall count
Nearest multi-notice firms by distinct-event totals (252 here — heavy-book).
Similar medical devices volume
Nearest multi-notice firms in the same narrow category lane.
Frequently Asked Questions
How many federal recall notices name Maquet Cardiovascular, LLC? ▼
PlainRecalls indexes 252 distinct federal recall events naming Maquet Cardiovascular, LLC, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Maquet Cardiovascular, LLC sit among other recalling firms? ▼
Maquet Cardiovascular, LLC ranks #52 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Maquet Cardiovascular, LLC's notices? ▼
FDA Devices accounts for 252 of this firm's 252 indexed notices.
What product category dominates Maquet Cardiovascular, LLC's filing book? ▼
Filings for Maquet Cardiovascular, LLC span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Maquet Cardiovascular, LLC: 252 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.
Firm-level totals aggregate distinct federal recall events naming Maquet Cardiovascular, LLC; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026