Manufacturer

TELEFLEX LLC

140 recalls in our database name TELEFLEX LLC as the manufacturing or recalling firm.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–25 of 140

HighFDA (Devices)·Z-2639-2026·2026-07-08
Pilling Wecksorb Neurosponges Surgical Sponges Recalled for Endotoxin Contamination
Teleflex LLC is recalling Pilling Wecksorb Neurosponges and Neurosponge Strips due to out-of-specification or potentially out-of-specification endotoxin levels. The cotton surgical sponges are used in brain and spine surgery.
Product
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 V
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2097-2023·2023-07-12
Teleflex Pilling Surgical Retractor Recalled for Incomplete Cleaning Instructions
Teleflex recalls the Pilling LOWSLEY PROSTATIC TRACTOR STR due to incomplete pre-cleaning instructions in the product manual. The issue affects 32 units distributed nationwide and internationally.
Product
Pilling LOWSLEY PROSTATIC TRACTOR STR, REF 243201; retractor
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2095-2023·2023-07-12
Teleflex Pilling O'Reilly Esophageal Retractor Recalled for Incomplete Cleaning Instructions
TELEFLEX LLC recalled the Pilling O'REILLY ESOPHAGEAL RETRACTOR (REF 381801A) due to incomplete pre-cleaning instructions in the product's Instructions for Use. The recall affects 365 units distributed nationwide and internationally.
Product
Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2096-2023·2023-07-12
Teleflex Surgical Retractor Recalled for Incomplete Pre-Cleaning Instructions
Teleflex LLC is recalling 170 units of the Pilling Lowsley Prostatic Retractor due to incomplete pre-cleaning instructions in the user manual. Incomplete instructions may prevent proper sterilization of the surgical instrument.
Product
Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1876-2023·2023-07-05
Endotracheal Tube Connector Disconnection Recall — FDA Class I
TELEFLEX endotracheal tubes (Murphy design) may have a disconnected 15mm connector. Approximately 12,382 affected units were distributed nationwide. Healthcare facilities should inspect tubes before use.
Product
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382050
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1898-2023·2023-07-05
RUSCHELIT Safety Clear Tracheal Tube 15mm Connector Disconnection Recall
TELEFLEX is recalling RUSCHELIT Safety Clear Tracheal Tubes due to reported disconnection of the 15mm connector, affecting approximately 37,076 units distributed nationwide.
Product
RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480040
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1828-2023·2023-07-05
Teleflex Slick Set endotracheal tubes recalled for connector disconnection
Teleflex Slick Set endotracheal tubes (REF 170055) are being recalled by the FDA following reports of disconnection of the 15mm connector. This Class I recall affects approximately 3,530 units distributed nationwide.
Product
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170055
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1882-2023·2023-07-05
TELEFLEX Endotracheal Tubes Recalled Due to Connector Disconnection Risk
TELEFLEX is recalling 760 endotracheal tubes due to reports of 15mm connector disconnection. This medical device failure could compromise airway management during critical care.
Product
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080095
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1947-2023·2023-07-05
Preformed AGT Endotracheal Tubes Recalled Due to Connector Disconnection
Teleflex is recalling 25,520 Preformed AGT endotracheal tubes due to reports of 15mm connector disconnection. This is an FDA Class I recall affecting units distributed nationwide.
Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780070
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1841-2023·2023-07-05
Slick Set Uncuffed Endotracheal Tube Connector Disconnection Recall
Teleflex LLC is recalling approximately 10,650 units of Slick Set Uncuffed Endotracheal Tubes due to reports of 15mm connector disconnection from the tube.
Product
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170140
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1927-2023·2023-07-05
Endotracheal Tubes Recalled for Connector Disconnection Risk
Teleflex LLC is recalling 2,860 endotracheal tubes due to reports of 15mm connector disconnection. Affected tubes were distributed nationwide including Puerto Rico.
Product
Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380035
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1890-2023·2023-07-05
Teleflex endotracheal tubes recalled for connector disconnection defect
Teleflex LLC is recalling 170,179 endotracheal tubes nationwide due to reports of 15mm connector disconnection. The tubes are used for airway management in medical facilities.
Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082080
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1893-2023·2023-07-05
Teleflex Endotracheal Tubes Recalled Due to Connector Disconnection Risk
Teleflex is recalling 18,620 endotracheal tubes due to reported disconnection of 15mm connectors. The tubes are used for oral and nasal intubation and were distributed nationwide.
Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082095
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1874-2023·2023-07-05
Endotracheal Tube Recall Due to 15mm Connector Disconnection
TELEFLEX is recalling endotracheal tubes due to reports of 15mm connector disconnection. Approximately 25,160 units were distributed nationwide.
Product
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382030
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1858-2023·2023-07-05
Flexi-Set Endotracheal Tubes recalled due to connector disconnection risk
Teleflex is recalling 12,400 Flexi-Set Uncuffed Endotracheal Tube and Stylet Sets nationwide due to reports of 15mm connector disconnection. The affected batches and lot numbers are identified above.
Product
Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506545
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1940-2023·2023-07-05
Endotracheal Tube 15mm Connector Disconnection Recall
Teleflex is recalling endotracheal tubes after reports that the 15mm connector may disconnect from the tube. The recall affects 36,135 units distributed nationwide.
Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780035
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1961-2023·2023-07-05
TELEFLEX Endotracheal Tubes Recalled for Connector Disconnection Risk
TELEFLEX is recalling 17,950 endotracheal tubes due to reports of the 15mm connector disconnecting from the device. These are critical airway support devices.
Product
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080070
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1851-2023·2023-07-05
Flexi-Set Endotracheal Tube Connector May Disconnect During Use
Teleflex is recalling 244,120 Flexi-Set Cuffed Endotracheal Tubes due to reports that the 15mm connector may disconnect from the tube. Affected units were distributed nationwide.
Product
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504580
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1891-2023·2023-07-05
Teleflex Endotracheal Tubes Recalled for 15mm Connector Disconnection
Teleflex is recalling approximately 39,550 endotracheal tubes due to reports of 15mm connector disconnection. The FDA Class I recall affects units distributed nationwide including Puerto Rico.
Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082085
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1886-2023·2023-07-05
Teleflex Endotracheal Tubes Recalled for Connector Disconnection Risk
Teleflex is recalling approximately 170,610 endotracheal tubes due to reports of 15mm connector disconnection. The disconnection could compromise airway management during mechanical ventilation.
Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082060
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1839-2023·2023-07-05
Endotracheal Tube Connector Disconnection Risk Prompts Teleflex Recall
Teleflex is recalling Slick Set Uncuffed Endotracheal Tubes due to reported 15mm connector disconnection. The recall affects 22,400 units distributed nationwide.
Product
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170130
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1889-2023·2023-07-05
Endotracheal Tube Connectors Recalled for Potential Disconnection Risk
TELEFLEX LLC is recalling 300,613 endotracheal tubes due to reports of 15mm connector disconnection. The affected tubes were distributed nationwide and could pose patient safety risks.
Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082075
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1934-2023·2023-07-05
Endotracheal Tubes With 15mm Connector Disconnection Recalled Nationwide
TELEFLEX is recalling 25,630 endotracheal tubes nationwide because the 15mm connector can disconnect. The affected products were distributed throughout the United States and Puerto Rico.
Product
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382025
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1894-2023·2023-07-05
Endotracheal tubes recalled for 15mm connector disconnection
Teleflex is recalling 19,250 endotracheal tubes because the 15mm connector may disconnect during use, potentially compromising airway management in patients.
Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082100
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1853-2023·2023-07-05
Flexi-Set Cuffed Endotracheal Tube and Stylet Connector Disconnection Recall
TELEFLEX LLC is recalling 13,710 units of Flexi-Set Cuffed Endotracheal Tubes due to reports of connector disconnection. The 15mm connector may separate from the tube during use.
Product
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504590
Category
Medical Device
Distribution
Distributed nationwide