PlainRecalls

Maquet Cardiovascular, LLC

Compiled from official public sources by the editorial team.

251 recalls on record · Latest: Oct 1, 2025

Maquet Cardiovascular, LLC Recall Insight

Maquet Cardiovascular, LLC appears on 251 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.247% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Oct 1, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 5 critical, 45 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from May 13, 2020 to Oct 1, 2025.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

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-60…

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…

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 …

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 allow…

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…

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…

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 Hem…

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…

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…

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. …

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 car…

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 surfa…

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 affecte…

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 o…

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 o…

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 o…

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 …

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 replaceme…

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 …

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 o…

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 o…

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 o…

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 o…

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 …

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 …

FDA Devices Moderate May 13, 2020

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch, Product Code: M00202175734P0 - Product Usage: for use in the replacement or repair …

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.