PlainRecalls

CardioQuip, LLC

Compiled from official public sources by the publisher.

9 recalls on record · Latest: Dec 27, 2023

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Agency notice ledger

Federal filing book CardioQuip, LLC LIGHT-BOOK · SINGLE-AGENCY

#1,575 of 14,151 · 9 notices · 0.009% archive

  • BOOK 9 notices
  • RANK #1,575 of 14,151
  • SHARE 0.009% archive
  • AGENCY FDA Devices (9)
  • CAT medical devices
  • CATS 1 category
  • LATEST Dec 27, 2023
  • PHOTO 3Cs Organics LLC

Nearest notice-volume peer: 3Cs Organics LLC (0 notice gap)

CardioQuip, LLC accounts for about 0.009% of the 104,423-notice archive on 9 distinct filings — a mid 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 CardioQuip, LLC compares to 14,151 recalling firms

CardioQuip, LLC ranks 1,575th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

CardioQuip, LLC vs all firms by recall-notice count

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

9 1575th of 14151 higher than 12,464 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

CardioQuip, LLC in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows CardioQuip, LLC holds about 0.009% of archive notices alongside 9 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Dec 27, 2023

CardioQuip Modular Cooler-Heater, Model: MCH-1000(m), Power: 115V-60Hz, 16A
FDA Devices Moderate Dec 27, 2023

CardioQuip Modular Cooler-Heater, Model: MCH-1000(i), Power: 115V-60Hz, 16A
FDA Devices Moderate Dec 13, 2023

CardioQuip Modular Cooler-Heater, Model:MCH-1000(i), Power: 115V-60hz,16A
FDA Devices Moderate Dec 13, 2023

CardioQuip Modular Cooler-Heater, Model:MCH-1000(m), Power: 115V-60hz,16A
FDA Devices Moderate Oct 13, 2021

CardioQuip, Modular Cooler-Heater, Model: MCH-1000(i), CE 2797, UDI: (01)00860000846103
FDA Devices Moderate Oct 13, 2021

CardioQuip, Modular Cooler-Heater 1000(i), Refrigeration Module, Model: MCH-10RMS, UDI: (01)00860000846127 used with heat exchange devices.
FDA Devices Moderate Oct 13, 2021

CardioQuip, Modular Cooler-Heater 1000(m),Thermoelectric Cooling Lid, Model: MCH-11TEC,CE 2797, UDI: (01) 00860000846134
FDA Devices Moderate Oct 13, 2021

CardioQuip, Modular Cooler-Heater 1000(m),Compact Unit, Model:MCH-1000(m),CE 2797, UDI: (01)00860000846110
FDA Devices Moderate Oct 13, 2021

CardioQuip, Modular Cooler-Heater 1000(i), Standard Unit, Model: MCH-10RMS, CE 2797, UDI: (01) 00860000846127

CardioQuip, LLC holds a measurable archive slice

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 CardioQuip, LLC? ▼
PlainRecalls indexes 9 distinct federal recall events naming CardioQuip, 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 CardioQuip, LLC sit among other recalling firms? ▼
CardioQuip, LLC ranks #1,575 of 14,151 by distinct recall-event count among 14,151 firms in this archive (88th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of CardioQuip, LLC's notices? ▼
FDA Devices accounts for 9 of this firm's 9 indexed notices.
What product category dominates CardioQuip, LLC's filing book? ▼
Filings for CardioQuip, 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.
CardioQuip, LLC: 9 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 CardioQuip, LLC; individual notices remain authoritative on each linked recall page.

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