PlainRecalls

Terumo Medical Corporation

Compiled from official public sources by the publisher.

19 recalls on record · Latest: Aug 19, 2026

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Agency notice ledger

Federal filing book Terumo Medical Corporation LIGHT-BOOK · SINGLE-AGENCY

#866 of 14,151 · 19 notices · 0.018% archive

  • BOOK 19 notices
  • RANK #866 of 14,151
  • SHARE 0.018% archive
  • AGENCY FDA Devices (19)
  • CAT medical devices
  • CATS 1 category
  • LATEST Aug 19, 2026
  • PHOTO Abbott

Nearest notice-volume peer: Abbott (0 notice gap)

Terumo Medical Corporation accounts for about 0.018% of the 104,423-notice archive on 19 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 Terumo Medical Corporation compares to 14,151 recalling firms

Terumo Medical Corporation ranks 866th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Terumo Medical Corporation vs all firms by recall-notice count

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

19 866th of 14151 higher than 13,281 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 Medical Corporation in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Terumo Medical Corporation holds about 0.018% of archive notices alongside 19 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Aug 19, 2026

GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to facilitate placing a catheter through the skin into the radial artery.
FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 25G x 5/8", Product Code 100280
FDA Devices Moderate Jul 31, 2019

Terumo Needle, 23G x 1", Product Code NN2325R
FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 20G x 1", Product Code 100204
FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 22G x 1", Product Code 100211
FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 22G x 3/4", Product Code 100215
FDA Devices Moderate Jul 31, 2019

Terumo Needle, 18G x 1", Product Code NN1825R
FDA Devices Moderate Jul 31, 2019

Terumo Needle, 30G x 1/2", Product Code NN3013R
FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 22G x 3/4", Product Code 100279
FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 25G x 5/8", Product Code 100220
FDA Devices Critical Jun 5, 2019

SOLOPATH Balloon Expandable TransFemoral System, Model Numbers STFI-1425, STFI-1435, STFI-1625, STFI-1635, STFI-1825, STFI-1835, STFI-1925, STFI-1935, STFI-2125, STFI-2135 Product Usage: The SoloPath Balloon Expandable TransFemoral Introducer System (STFI) and the SoloPath¿ Re-Collapsible Access System are sterile, single use devices designed for low profile, large bore vessel access. Both SoloPath products are inserted percutaneously into the femoral artery, over a guidewi
FDA Devices Critical Jun 5, 2019

Portico Solo Re-Collapsible Access System , Model Numbers PRTSOLO-19, PRTSOLO-20
FDA Devices Critical Jun 5, 2019

SOLOPATH Re-Collapsible Access System, Model Numbers SR-1925, SR-1935, SR-2025, SR-2035, SR-2225, SR-2235, SR-2425, SR-2435
FDA Devices Moderate Mar 7, 2018

Destination Guiding Sheath catheter introducer, Catalog Number: RSR06 Product Usage: The Destination¿ Guiding Sheath is designed to be used for the introduction of interventional and diagnostic devices into the human vasculature, including but not limited to the renal, carotid, and peripheral arteries.
FDA Devices Moderate May 10, 2017

Destination Renal Guiding Sheath Intended for the introduction of interventional and diagnostic devices into the human vasculature.
FDA Devices Moderate May 10, 2017

SurFlo IV Catheter
FDA Devices Moderate Sep 14, 2016

PINNACLE¿ Introducer Sheath PINNACLE PRECISION ACCESS SYSTEM¿ Sheath PINNACLE¿ TIF TIP" Introducer Sheath PINNACLE¿ R/O II Radiopaque Marker Introducer Sheath
FDA Devices Moderate Jul 3, 2013

Pinnacle¿ Destination¿ Peripheral Guiding Sheath, 8 French, 90cm, Straight Tip, Cross Cut Valve. Acts as a conduit to facilitate the introduction of interventional and diagnostic devices into the human vasculature.
FDA Devices Moderate Jul 3, 2013

Terumo Glidesheath (tm), 6 French, Nitinol wire, product code 15-1060. Used to facilitate placing a catheter through the skin into a vein or artery.

Terumo Medical Corporation holds a measurable archive slice

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

Similar recall count

Nearest multi-notice firms by distinct-event totals (19 here).

Abbott 19 Abbott Gmbh & Co. Kg 19 Abbott Medical Optics Inc. (Amo) 19 Adm Milling 19 Advance Pierre N 19

Similar medical devices volume

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

Abbott 19 Abbott Gmbh & Co. Kg 19 Abbott Medical Optics Inc. (Amo) 19 Amo Puerto Rico Manufacturing, Inc. 19

Frequently Asked Questions

How many federal recall notices name Terumo Medical Corporation? ▼
PlainRecalls indexes 19 distinct federal recall events naming Terumo Medical 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 Medical Corporation sit among other recalling firms? ▼
Terumo Medical Corporation ranks #866 of 14,151 by distinct recall-event count among 14,151 firms in this archive (94th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Terumo Medical Corporation's notices? ▼
FDA Devices accounts for 19 of this firm's 19 indexed notices.
What product category dominates Terumo Medical Corporation's filing book? ▼
Filings for Terumo Medical 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 Medical Corporation: 19 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 Medical Corporation; individual notices remain authoritative on each linked recall page.

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