PlainRecalls

Teleflex, Inc.

Compiled from official public sources by the publisher.

11 recalls on record · Latest: Aug 26, 2015

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Agency notice ledger

Federal filing book Teleflex, Inc. LIGHT-BOOK · SINGLE-AGENCY

#1,403 of 14,151 · 11 notices · 0.011% archive

  • BOOK 11 notices
  • RANK #1,403 of 14,151
  • SHARE 0.011% archive
  • AGENCY FDA Devices (11)
  • CAT medical devices
  • CATS 1 category
  • LATEST Aug 26, 2015
  • PHOTO Agfa Corp.

Nearest notice-volume peer: Agfa Corp. (0 notice gap)

Teleflex, Inc. accounts for about 0.011% of the 104,423-notice archive on 11 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 →

Teleflex, Inc.'s standing among 14,151 recalling firms

Teleflex, Inc. ranks 1,403rd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Teleflex, Inc. vs all firms by recall-notice count

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

11 1403rd of 14151 higher than 12,735 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, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Teleflex, Inc. holds about 0.011% of archive notices alongside 11 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Aug 26, 2015

Carlens Bronchial Double Lumen Tube Set (Left) Sterile
FDA Devices Moderate Aug 26, 2015

Bronchial Double Lumen Tube Set (Right), Sterile
FDA Devices Moderate Aug 26, 2015

Bronchial One Lumen Tube - Left
FDA Devices Moderate Aug 26, 2015

Bronchial Double Lumen Tube Set (Left), Sterile
FDA Devices Moderate Aug 26, 2015

Bronchial One Lumen Tube - Right
FDA Devices Moderate Aug 26, 2015

Tracheopart Set (Right), Sterile
FDA Devices Moderate Aug 26, 2015

Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile
FDA Devices Moderate Aug 26, 2015

White Bronchial Double Lumen Tube Set (Right) Sterile
FDA Devices Moderate Aug 26, 2015

Tracheopart Set (Left), Sterile
FDA Devices Moderate Feb 25, 2015

R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated for airway management. The product may be used to reduce the potential for kinking whenever an unusual positioning of the head or neck is required following intubation.
FDA Devices Critical Feb 18, 2015

MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. A heat and moisture condenser (artificial nose) is a device intended to be positioned over a tracheotomy (a surgically created opening in the throat) or tracheal tube (a tube inserted into the trachea) to warm and humidify gases breathed in by a patient.

Teleflex, Inc. 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 (11 here — thin-book).

Agfa Corp. 11 Ajinomoto Foods North America Inc. 11 Akron Pharma, Inc. 11 Amendia, Inc 11 Aniara Diagnostica LLC 11

Similar medical devices volume

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

Agfa Corp. 11 Amendia, Inc 11 Aniara Diagnostica LLC 11 Arjohuntleigh Polska Sp. z.o.o. 11

Frequently Asked Questions

How many federal recall notices name Teleflex, Inc.? ▼
PlainRecalls indexes 11 distinct federal recall events naming Teleflex, Inc., 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, Inc. sit among other recalling firms? ▼
Teleflex, Inc. ranks #1,403 of 14,151 by distinct recall-event count among 14,151 firms in this archive (90th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Teleflex, Inc.'s notices? ▼
FDA Devices accounts for 11 of this firm's 11 indexed notices.
What product category dominates Teleflex, Inc.'s filing book? ▼
Filings for Teleflex, 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.
Teleflex, Inc.: 11 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, Inc.; individual notices remain authoritative on each linked recall page.

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