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 50 entries, severity tagging shows 47 critical, 3 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 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 (50). The date window on this page runs from Jul 5, 2023 to Jul 12, 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 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

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170145

Nearby Manufacturers

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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