PlainRecalls

Teleflex Medical

Compiled from official public sources by the publisher.

204 recalls on record · Latest: Jan 22, 2020

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Agency notice ledger

Federal filing book Teleflex Medical HEAVY-BOOK · SINGLE-AGENCY

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

  • BOOK 204 notices
  • RANK #68 of 14,151
  • SHARE 0.195% archive
  • AGENCY FDA Devices (204)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jan 22, 2020
  • PHOTO Terumo Cardiovascular…

Nearest notice-volume peer: Terumo Cardiovascular Systems Corporation (0 notice gap)

Teleflex Medical 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 →

Where Teleflex Medical sits among 14,151 recalling firms

Teleflex Medical ranks 68th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Teleflex Medical vs all firms by recall-notice count

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

204 68th 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

Teleflex Medical in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Teleflex Medical 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 May 1, 2013

Belly Bag Urine Collection Bag with Hip Belt. The product is a sterile urine collection device that collects urine by mechanical means when attached to an indwelling Foley or suprapubic catheter.
FDA Devices Moderate Oct 24, 2012

Hem-o-lok Large Polymer Ligating Clips, REF #544240, Rx only, Sterile, Teleflex Medical, Research Triangle Park, NC 27709. Teleflex Medicals Hem-o-lok polymer ligating clips are single use, sterile, non-absorbable medial devices that have been designed to ligate vessels and tissue structures during various types of surgical procedures. Vessels and tissue structures in the range of 0.5 to 16 mm can be effectively ligated with Hem-o-lok clips.
FDA Devices Low Aug 22, 2012

TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical, Research Triangle Park, NC. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into the body.
FDA Devices Moderate Jul 25, 2012

Hudson RCI Concha Therm Neptune Humidifier, Rx Only, Product Usage: Usage: Device that is intended to add moisture to, and sometime to warm, the breathing gases for administration to a patient.

Teleflex Medical 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 Teleflex Medical? ▼
PlainRecalls indexes 204 distinct federal recall events naming Teleflex Medical, 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 Teleflex Medical sit among other recalling firms? ▼
Teleflex Medical ranks #68 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 Teleflex Medical's notices? ▼
FDA Devices accounts for 204 of this firm's 204 indexed notices.
What product category dominates Teleflex Medical's filing book? ▼
Filings for Teleflex Medical 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.
Teleflex Medical: 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 Teleflex Medical; individual notices remain authoritative on each linked recall page.

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