PlainRecalls

Terumo Cardiovascular Systems Corporation

Compiled from official public sources by the publisher.

204 recalls on record · Latest: Jul 2, 2025

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Agency notice ledger

Federal filing book Terumo Cardiovascular Syste… HEAVY-BOOK · SINGLE-AGENCY

#69 of 14,151 · 204 notices · 0.195% archive

  • BOOK 204 notices
  • RANK #69 of 14,151
  • SHARE 0.195% archive
  • AGENCY FDA Devices (204)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 2, 2025
  • PHOTO Teleflex Medical

Nearest notice-volume peer: Teleflex Medical (0 notice gap)

Terumo Cardiovascular Systems Corporation accounts for about 0.195% of the 104,423-notice archive on 204 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 →

Terumo Cardiovascular Syste…'s standing among 14,151 recalling firms

Terumo Cardiovascular Systems Corporation ranks 69th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Terumo Cardiovascular Syste… vs all firms by recall-notice count

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

204 69th of 14151 higher than 14,082 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

Terumo Cardiovascular Syste… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Terumo Cardiovascular Systems Corporation holds about 0.195% of archive notices alongside 204 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jun 27, 2012

SARNS FLEXIBLE ARTERIAL CANNULA: 6.7 MM (20 FR) 00 WITH 3/8" CONNECTOR,SUTURE RING, 9.5" (24 CM) LONG. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.
FDA Devices Moderate Jun 27, 2012

CPB CATHETER KIT- DR.VAN TRIGHT. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.
FDA Devices Moderate Jun 27, 2012

CUSTOM CPB CATHETER KIT-DR. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.
FDA Devices Moderate Jun 27, 2012

SPECIALTYCARE - HUDGENS. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.

Terumo Cardiovascular Syste… carries an outsized archive share

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 Terumo Cardiovascular Syste…? ▼
PlainRecalls indexes 204 distinct federal recall events naming Terumo Cardiovascular Systems Corporation, 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 Terumo Cardiovascular Syste… sit among other recalling firms? ▼
Terumo Cardiovascular Systems Corporation ranks #69 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Terumo Cardiovascular Syste…'s notices? ▼
FDA Devices accounts for 204 of this firm's 204 indexed notices.
What product category dominates Terumo Cardiovascular Syste…'s filing book? ▼
Filings for Terumo Cardiovascular Systems Corporation 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.
Terumo Cardiovascular Systems Corporation: 204 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 Terumo Cardiovascular Systems Corporation; individual notices remain authoritative on each linked recall page.

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