PlainRecalls

Teleflex LLC

140 recalls on record · Latest: Jul 8, 2026

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Agency notice ledger

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

#116 of 14,151 · 140 notices · 0.134% archive

  • BOOK 140 notices
  • RANK #116 of 14,151
  • SHARE 0.134% archive
  • AGENCY FDA Devices (140)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 8, 2026
  • PHOTO First Royal Care Co.…

Nearest notice-volume peer: First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy (0 notice gap)

Teleflex LLC accounts for about 0.134% of the 104,423-notice archive on 140 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 →

Teleflex LLC's standing among 14,151 recalling firms

Teleflex LLC ranks 116th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Teleflex LLC vs all firms by recall-notice count

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

140 116th of 14151 higher than 14,035 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 LLC in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Teleflex LLC holds about 0.134% of archive notices alongside 140 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jul 8, 2026

Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips (Cotton) Model/Catalog Number: 200100 200101 200102 200103 200104 200105 200106 200108 200110 200112 200120 200121 200123 200131 Software Version: N/A Product Description: Wecksorb Neurosponges are made of an absorbent cotton material. Certain Neurosponge varieties are available with an x-ray detectable thread to assist with location within the surgical si

FDA Devices Moderate Jul 12, 2023

Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor

FDA Devices Moderate Jul 12, 2023

Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor

FDA Devices Moderate Jul 12, 2023

Pilling LOWSLEY PROSTATIC TRACTOR STR, REF 243201; retractor

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170085

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382035

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382055

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082075

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150055

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181055

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082090

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380065

FDA Devices Critical Jul 5, 2023

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480030

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080060

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180070

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380050

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780085

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380030

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170140

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780060

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150025

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181045

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080100

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170080

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170090

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780075

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170065

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180050

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082060

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781060

FDA Devices Critical Jul 5, 2023

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480035

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781080

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382030

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080050

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170060

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170130

FDA Devices Critical Jul 5, 2023

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504560

FDA Devices Critical Jul 5, 2023

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506545

FDA Devices Critical Jul 5, 2023

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506550

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181040

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082065

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781075

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181050

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181060

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380060

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080080

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180060

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380055

Teleflex LLC 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 LLC?
PlainRecalls indexes 140 distinct federal recall events naming Teleflex LLC, 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 LLC sit among other recalling firms?
Teleflex LLC ranks #116 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 LLC's notices?
FDA Devices accounts for 140 of this firm's 140 indexed notices.
What product category dominates Teleflex LLC's filing book?
Filings for Teleflex LLC 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 LLC: 140 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 LLC; individual notices remain authoritative on each linked recall page.

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