TELEFLEX LLC recalls
Every recall we track for TELEFLEX LLC — 140 in all, from 2022–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from TELEFLEX LLC peaked in 2023 (128); 140 since 2017. 1% rated “stop using now”.
All FDA recall records for TELEFLEX LLC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 7 | 3 | 1 | 11 |
| 2023 | 1 | 118 | 9 | 0 | 128 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 1 | 1 |
Most common reasons for TELEFLEX LLC recalls
What to do if you have a recalled TELEFLEX LLC product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All TELEFLEX LLC recalls
9 shown- UnratedMedical device
TELEFLEX LLC recalls Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips
Recall of 1,481,700 US units of Pilling Wecksorb Neurosponges (cotton) due to potential endotoxin levels. Affected models include 200100-200131 with specific UDI codes and batch numbers. No remedy stated in official notice.
Pilling WecksorbMay 7, 2026 - Lower riskMedical device
TELEFLEX LLC recalls Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor
Teleflex recalls specific model Pilling Lowsley Prostatic Tractor CVD retractors due to incomplete pre-cleaning instructions in the manual. Affected units have lot numbers C7 through W1. Consumers should check their product details and contact Teleflex for guidance.
TeleflexMay 25, 2023 - Use cautionMedical device
TELEFLEX LLC recalls Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170085
Teleflex recalls Slick Set Cuffed Endotracheal Tubes with risk of 15mm connector disconnection. Affected products include specific batch numbers and model REF 170085.
TeleflexMay 25, 2023 - Use cautionMedical device
TELEFLEX LLC recalls Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that
Teleflex recalls Horizon Microclip Titanium Ligating Clips with missing safety feature that may cause improper vessel ligation during surgery. Affected units have specific lot numbers and UDI/DI codes.
TeleflexApr 28, 2023 - Lower riskMedical device
TELEFLEX LLC recalls Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat, REF 4000; for sealing residual oozing of tissue
Teleflex recalls D-Stat Flowable Hemostat (REF 4000) with expired diluent vials that may compromise sterility. Affected units have specific lot numbers and expiration dates. Consumers should check their product details.
TeleflexApr 12, 2023 - Use cautionMedical device
TELEFLEX LLC recalls Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal; b.
Teleflex recalls specific endotracheal tubes due to potential pilot balloon non-inflation or cuff non-deflation during intubation procedures.
TeleflexDec 8, 2022 - Lower riskMedical device
TELEFLEX LLC recalls Pilling Wecksorb Cylindrical Sponges
Teleflex recalls specific lots of Pilling Wecksorb Cylindrical Sponges due to potential sterility issues from unirradiated products. Affected items may not be sterile, posing infection risks.
TeleflexSep 28, 2022 - Lower riskMedical device
TELEFLEX LLC recalls Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140
Teleflex recalls non-sterile Pocket Pac i.c. catheter kits that could cause infection. Affected units have specific model and serial numbers. Contact Teleflex for replacement.
TeleflexSep 20, 2022 - UnratedMedical device
TELEFLEX LLC recalls Iso-Gard Filter S, Tethered Cap, REF: a) 19211T, OUS only; b) 19212T, OUS only; Microbial medical gas filter, single-use
Teleflex recalls Iso-Gard Filter S, Tethered Cap models 19211T and 19212T (US only) due to incidents of device splitting or detaching during use. No remedy specified in official notice.
TeleflexAug 29, 2022
TELEFLEX LLC recall questions
How many recalls has TELEFLEX LLC had?
140 recalls from TELEFLEX LLC are on record with U.S. safety agencies, from 2022–2026.
What is the most recent TELEFLEX LLC recall?
TELEFLEX LLC recalls Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips, dated May 7, 2026. Every TELEFLEX LLC recall is listed on this page, newest first.
Why are TELEFLEX LLC products recalled?
The most common reasons on record: Incidents of device splitting or detaching during use (6); Potential for pilot balloon non-inflation or cuff non-deflation. (3).
What should I do if I have a recalled TELEFLEX LLC product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new TELEFLEX LLC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.