PlainRecalls

TELEFLEX LLC

91 recalls on record · Latest: Jul 12, 2023

TELEFLEX LLC Recall Insight

TELEFLEX LLC appears on 91 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.108% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Jul 12, 2023, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 41 entries, severity tagging shows 35 critical, 6 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 41 of 41 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (41). The date window on this page runs from Oct 26, 2022 to Jul 5, 2023.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380025

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180065

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780080

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170095

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382065

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170155

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780055

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780090

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170120

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780035

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082080

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780040

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080075

FDA Devices Critical Jul 5, 2023

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480045

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082050

FDA Devices Critical Jul 5, 2023

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504585

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781055

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780065

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080055

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781070

FDA Devices Critical Jul 5, 2023

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504555

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080065

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780045

FDA Devices Critical Jul 5, 2023

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504580

FDA Devices Critical Jul 5, 2023

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506530

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170125

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150040

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382060

FDA Devices Critical Jul 5, 2023

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504590

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781050

FDA Devices Moderate Jun 7, 2023

Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that require vessel or tissue ligation

FDA Devices Moderate May 24, 2023

Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat, REF 4000; for sealing residual oozing of tissue tracts of femoral access sites …

FDA Devices Moderate Feb 1, 2023

Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal; b. Endotracheal Tube oral/nasal…

FDA Devices Moderate Feb 1, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation

FDA Devices Moderate Jan 4, 2023

Pilling Wecksorb Cylindrical Sponges

FDA Devices Moderate Nov 23, 2022

Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140 (IPN050116). Urinary catheter.

FDA Devices Critical Oct 26, 2022

Iso-Gard Filter S, Tethered Cap, REF: a) 19211T, OUS only; b) 19212T, OUS only; Microbial medical gas filter, single-use

FDA Devices Critical Oct 26, 2022

Iso-Gard Filter S, with Expandi-Flex, Tethered Cap, REF: a) 19261T, OUS only; b) 19262T, OUS only; c) 19272T, OUS only; Microbial medical gas filter…

FDA Devices Critical Oct 26, 2022

Iso-Gard Filter S, REF : a) 19211, OUS only; b) 19212; Microbial medical gas filter, single-use. Bacterial/viral filters for use in breathing syste…

FDA Devices Critical Oct 26, 2022

Filter + Catheter Mount, REF 191667-000100, OUS only. Catheter mount for circuit-patient connection (Endotracheal tube and mask)

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds