PlainRecalls

Cardiocommand Inc.

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Jul 24, 2019

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Agency notice ledger

Federal filing book Cardiocommand Inc. LIGHT-BOOK · SINGLE-AGENCY

#4,537 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #4,537 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 24, 2019
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company (0 notice gap)

Cardiocommand Inc. accounts for about 0.002% of the 104,423-notice archive on 2 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 Cardiocommand Inc. compares to 14,151 recalling firms

Cardiocommand Inc. ranks 4,537th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Cardiocommand Inc. vs all firms by recall-notice count

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

2 4537th of 14151 higher than 8,037 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 · 2026-10-29

Cardiocommand Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Cardiocommand Inc. holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of October 2026
FDA Devices Low Jul 24, 2019

TAPSYSTEM Model 2A, REF 8002A
FDA Devices Low Jun 19, 2019

CardioCommand, Inc. Transesophageal Cardiac Pacing and Recording System, Model 7A, REF 0101 - Product Usage: Indications for Use: - Temporary left atrial pacing to treat bradycardia, hypotension or AV junctional rhythm - Acceleration of heart rate as an alternative to exercise or drugs during diagnostic cardiac studies such as echocardiography or radionuclide ventriculography. - Antitachycardia pacing for cardioversion of supraventricular tachycardia (SVT), including atrial flutter and re-entran

Cardiocommand Inc. 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 Cardiocommand Inc.? ▼
PlainRecalls indexes 2 distinct federal recall events naming Cardiocommand Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of October 2026). That count is an issuance inventory, not a hazard score.
Where does Cardiocommand Inc. sit among other recalling firms? ▼
Cardiocommand Inc. ranks #4,537 of 14,151 by distinct recall-event count among 14,151 firms in this archive (57th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Cardiocommand Inc.'s notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Cardiocommand Inc.'s filing book? ▼
Filings for Cardiocommand Inc. 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.
Cardiocommand Inc.: 2 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 Cardiocommand Inc.; individual notices remain authoritative on each linked recall page.

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