PlainRecalls

Maquet Cardiovascular Us Sales, Llc

Compiled from official public sources by the publisher.

62 recalls on record · Latest: Dec 23, 2020

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Agency notice ledger

Federal filing book Maquet Cardiovascular Us Sa… MID-BOOK · SINGLE-AGENCY

#289 of 14,151 · 62 notices · 0.059% archive

  • BOOK 62 notices
  • RANK #289 of 14,151
  • SHARE 0.059% archive
  • AGENCY FDA Devices (62)
  • CAT medical devices
  • CATS 1 category
  • LATEST Dec 23, 2020
  • PHOTO Edge Pharma, LLC

Nearest notice-volume peer: Edge Pharma, LLC (0 notice gap)

Maquet Cardiovascular Us Sales, Llc accounts for about 0.059% of the 104,423-notice archive on 62 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 →

How Maquet Cardiovascular Us Sa… compares to 14,151 recalling firms

Maquet Cardiovascular Us Sales, Llc ranks 289th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Maquet Cardiovascular Us Sa… vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

62 289th of 14151 higher than 13,861 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 Us Sa… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Maquet Cardiovascular Us Sales, Llc holds about 0.059% of archive notices alongside 62 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Dec 31, 2014

Maquet Quadrox-ID Pediatric Diffusion Membrane Oxygenator with Bioline Coating; Part Number BEQ-HMOD-30000 For cardiac surgery in combination with a heart lung machine to oxygenate blood, remove carbon dioxide and adjust blood temperature.
FDA Devices Moderate Nov 19, 2014

Cardiohelp-I System Product Usage: A blood oxygenation and carbon dioxide removal system used to pump blood thorough the extracorporeal bypass circuit for circulatory and/or pulmonary support during procedures requiring cardiopulmonary bypass (for periods up to six hours). It is also intended to provide circulatory and/or pulmonary support during procedures not requiring cardiopulmonary bypass (for periods up to six hours).
FDA Devices Moderate Mar 19, 2014

MAQUET PLEGIOX Cardioplegia Heat Exchanger The PLEGIOX Cardioplegia Heat Exchanger is used as part of a cardioplegia system to set and maintain temperature for given flow rates and within the given temperature range of blood cardioplegic and crystalloid cardioplegic solutions during extracorporeal circulation. The product is designed for single use only, for an application period of no longer than 6 hours.
FDA Devices Moderate Feb 5, 2014

Compressor Mini To provide a supply of dry, filtered compressed air for a medical respiratory ventilator or anaesthesia machine that meet the specifications of the compressor mini. compressor mini is intended to be operated by healthcare providers, physicians, nurses, and technicians. Compressor mini is to be used only for bedside application within the hospital environment. Compressor mini is neither intended nor suitable for use during in-hospital patient transportation or during ambulance

FDA Devices Moderate Oct 2, 2013

QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator; QUADROX-i ADULT HMO 70000 / HMO 71000; QUADROX-iD Pediatric HMOD 30000. The QUADROX oxygenators are intended for use in extracorporeal circulation during cardiopulmonary bypass in cardiac surgery.
FDA Devices Moderate Oct 2, 2013

TEGRIS system Four labels of the Tegris System include: Emergency button (1703.72) MAQUET GmbH & Co. KG Kehler-Strabe 31 Baden-Wuerttemberg 76437 Rastatt, Germany Touch screen (elo) Elo TouchSystems 301 Constitution Drive Menlo Park, CA 94025 www.elotouch.com Manufacturer: Tyco Electronics Brand Name: Elo Touch Systems Made in China Tegris system (1703.01) MAQUET GmbH & Co. KG Kehler Strabe 31 76437 Rastatt, Germany OR Table Module (1703.71) MAQUET GmbH &

FDA Devices Moderate Jul 10, 2013

MAQUET Getinge Group Mobile Operating Table YUNO OTN GA 1433.01 EN 05. The YUNO OTN is used to support and position patients for surgical procedures immediately before, during and after the surgical phase. The table top is radio translucent and enables intraoperative use of X-ray equipment.
FDA Devices Moderate Jul 3, 2013

MAQUET GETINGE GROUP Arterial Cannula OD Used to introduce blood and sterile solutions into the systemic circulation during pediatric extracorporeal circulation procedures.
FDA Devices Critical May 8, 2013

Maquet Getinge Group battery modules for use with Maquet SERVO-i ventilator systems (Part #6487180). Battery for use with the SERVO-i Ventilator System. The SERVO-i Ventilator System is intended for treating and monitoring patients ranging from neonates to adults with respiratory failure or insufficiency. The ventilator is equipped with at least 2, NiMH battery modules (Part No. 6487180) which automatically supply 12V DC Power in case of an AC power failure, ensuring that ventilator settings

FDA Devices Moderate Feb 27, 2013

Maquet ELS Cannula 15 FR. Used for extracorporeal membrane oxygenation (ECMO) for the treatment of respiratory insufficiency in infants.
FDA Devices Moderate Nov 7, 2012

QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator; QUADROX-i ADULT HMO 70000 / HMO 71000; QUADROX-iD Pediatric HMOD 30000 Product Usage: The QUADROX oxygenators are intended for the use in extracorporeal circulation during cardiopulmonary bypass in cardiac surgery. Within the specified flow rate range, the device oxygenates the blood, eliminates carbon dioxide and regulates blood temperature. The devices utilization period is limited to six hours.
FDA Devices Critical Jul 18, 2012

FLOW-I Anesthesia System The system is intended for use in administrating anesthesia while controlling the entire ventilation for patients with no ability to breathe, as well as in supporting patients with a limited ability to breathe.

Maquet Cardiovascular Us Sa… 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 (62 here — heavy-book).

Edge Pharma, LLC 62 Vyaire Medical 62 Busse Hospital Disposables, Inc. 63 Giant Eagle, Inc. 63 Aesculap Implant Systems LLC 61

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Vyaire Medical 62 Busse Hospital Disposables, Inc. 63 Aesculap Implant Systems LLC 61 Philips Medical Systems, Inc. 65

Frequently Asked Questions

How many federal recall notices name Maquet Cardiovascular Us Sa…? ▼
PlainRecalls indexes 62 distinct federal recall events naming Maquet Cardiovascular Us Sales, 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 Us Sa… sit among other recalling firms? ▼
Maquet Cardiovascular Us Sales, Llc ranks #289 of 14,151 by distinct recall-event count among 14,151 firms in this archive (98th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Maquet Cardiovascular Us Sa…'s notices? ▼
FDA Devices accounts for 62 of this firm's 62 indexed notices.
What product category dominates Maquet Cardiovascular Us Sa…'s filing book? ▼
Filings for Maquet Cardiovascular Us Sales, 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 Us Sales, Llc: 62 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 Us Sales, Llc; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026