PlainRecalls

Maquet Cardiopulmonary Ag

Compiled from official public sources by the publisher.

5 recalls on record · Latest: Jun 4, 2025

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Agency notice ledger

Federal filing book Maquet Cardiopulmonary Ag LIGHT-BOOK · SINGLE-AGENCY

#2,549 of 14,151 · 5 notices · 0.005% archive

  • BOOK 5 notices
  • RANK #2,549 of 14,151
  • SHARE 0.005% archive
  • AGENCY FDA Devices (5)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 4, 2025
  • PHOTO A G Specialty Foods I…

Nearest notice-volume peer: A G Specialty Foods Inc (0 notice gap)

Maquet Cardiopulmonary Ag accounts for about 0.005% of the 104,423-notice archive on 5 distinct filings — a light 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 Cardiopulmonary Ag compares to 14,151 recalling firms

Maquet Cardiopulmonary Ag ranks 2,549th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Maquet Cardiopulmonary Ag vs all firms by recall-notice count

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

5 2549th of 14151 higher than 11,411 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 · 2026-09-15

Maquet Cardiopulmonary Ag in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Maquet Cardiopulmonary Ag holds about 0.005% of archive notices alongside 5 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jun 4, 2025

Cardiohelp System HKH 8820 Wall Holder. Mounting bracket designed to hold the CARDIOHELP-i system for interhospital transport by vehicle.
FDA Devices Moderate Jun 20, 2018

Aortic Arterial Cannula 22 Fr (O.D.); 23 cm (L); with 3/8-inch connector with LL, Part Number 701002246, Article Number A22-7107. For use in cardiopulmonary bypass
FDA Devices Moderate Jun 20, 2018

Aortic Arterial Cannula 20 Fr (O.D.); 23 cm (L); with 3/8-inch wide connector, Part Number 701002206, Article Number A20-0101. For use in cardiopulmonary bypass
FDA Devices Moderate Jun 20, 2018

Aortic Arterial Cannula 24 Fr (O.D.); 23 cm (L); with 3/8-inch connector with LL, Part Number 701002267, Article Number A24-7107. For use in cardiopulmonary bypass
FDA Devices Moderate May 16, 2018

CARDIOHELP Gas Bottle Holder HKH 8880, Product Code/Part Number 70105.0901 Product Usage: The Cardiohelp Gas Bottle (or Cylinder) Holder HKH 8880 is an accessory for the CARDIOHELP System and required for inter-hospital patient transport in aircraft and road vehicles (mobile intensive care units and ambulances). Inter-hospital patient transport is transport of the patient between clinics, where the clinical environment is left (e.g., transport in vehicles such as ambulances or aircraft). The

Maquet Cardiopulmonary Ag is a small archive contributor

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Frequently Asked Questions

How many federal recall notices name Maquet Cardiopulmonary Ag? ▼
PlainRecalls indexes 5 distinct federal recall events naming Maquet Cardiopulmonary Ag, 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 Cardiopulmonary Ag sit among other recalling firms? ▼
Maquet Cardiopulmonary Ag ranks #2,549 of 14,151 by distinct recall-event count among 14,151 firms in this archive (81st percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Maquet Cardiopulmonary Ag's notices? ▼
FDA Devices accounts for 5 of this firm's 5 indexed notices.
What product category dominates Maquet Cardiopulmonary Ag's filing book? ▼
Filings for Maquet Cardiopulmonary Ag 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 Cardiopulmonary Ag: 5 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 Cardiopulmonary Ag; individual notices remain authoritative on each linked recall page.

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