PlainRecalls

CardioTek Bv

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Jun 29, 2022

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Agency notice ledger

Federal filing book CardioTek Bv LIGHT-BOOK · SINGLE-AGENCY

#4,538 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #4,538 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 29, 2022
  • PHOTO 3M Company

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

CardioTek Bv 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 →

CardioTek Bv's standing among 14,151 recalling firms

CardioTek Bv ranks 4,538th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

CardioTek Bv vs all firms by recall-notice count

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

2 4538th 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 · 2026-09-15

CardioTek Bv in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows CardioTek Bv holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jun 29, 2022

CardioTek EP-TRACER Software V2.x.
FDA Devices Moderate Jul 12, 2017

CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is an electrophysiology measurement system used to acquire, filter, digitize, amplify, display, and record signals obtained during electrophysiological studies and related procedures. The system allows the user to monitor, display and record the signals. The system incorporates a stimulator intended to be used for diagnostic cardiac stimulation during electrophysiological testing of the heart.

CardioTek Bv is a small archive contributor

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

Similar medical devices volume

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

3M Company 2 3M Company/3m Espe Dental Products 2 A.o. Smith Electrical Products Co., of Tipp City, Ohio 2 Abbott GmbH 2

Frequently Asked Questions

How many federal recall notices name CardioTek Bv? ▼
PlainRecalls indexes 2 distinct federal recall events naming CardioTek Bv, 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 CardioTek Bv sit among other recalling firms? ▼
CardioTek Bv ranks #4,538 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 CardioTek Bv's notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates CardioTek Bv's filing book? ▼
Filings for CardioTek Bv 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.
CardioTek Bv: 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 CardioTek Bv; individual notices remain authoritative on each linked recall page.

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