Manufacturer
140 recalls in our database name TELEFLEX LLC as the manufacturing or recalling firm.
Of the 140 recalls from TELEFLEX LLC we have scored against our rubric, 10 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 119 (85%) are Severe.
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.
Teleflex is recalling endotracheal tubes due to reports of 15mm connector disconnection. The FDA Class I recall affects approximately 30,423 units distributed nationwide.
Teleflex is recalling 3,370 endotracheal tubes nationwide after reports of disconnection of the 15mm connector. Disconnection during use could interrupt airway access.
Teleflex is recalling 12,852 units of Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection from the tube. Affected units were distributed nationwide including Puerto Rico.
TELEFLEX LLC is recalling 2,140 endotracheal tubes nationwide due to reports of the 15mm connector disconnecting from the tube. Affected units were distributed throughout the United States, including Puerto Rico.
TELEFLEX LLC recalls Flexi-Set Uncuffed Endotracheal Tube and Stylet Sets due to reports of the 15mm connector disconnecting from the tube. Approximately 16,400 units distributed nationwide are affected.
TELEFLEX LLC is recalling 1,280 endotracheal tubes due to reports of 15mm connector disconnection. The defect could compromise airway management and poses serious safety risks during medical procedures.
Teleflex is recalling Preformed AGT Oral Endotracheal Tubes due to reports of the 15mm connector disconnecting from the tube. Approximately 2,980 units were distributed nationwide.
TELEFLEX is recalling 17,950 endotracheal tubes due to reports of the 15mm connector disconnecting from the device. These are critical airway support devices.
Teleflex is recalling 37,890 Preformed AGT endotracheal tubes due to reports of 15mm connector disconnection. The devices were distributed nationwide in the United States and Puerto Rico.
Teleflex endotracheal tubes with specific batch numbers may experience disconnection of the 15mm connector during clinical use. The FDA has classified this as a Class I recall affecting 247,645 units distributed 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.
Teleflex has recalled 49,050 endotracheal tubes due to reported disconnection of the 15mm connector. Affected units were distributed nationwide, including Puerto Rico.
Teleflex is recalling Slick Set Uncuffed Endotracheal Tube and Stylet Sets due to reports that the 15mm connector may disconnect from the tube. The recall affects 447 units distributed nationwide.
Teleflex is recalling 18,353 Flexi-Set Uncuffed Endotracheal Tube sets nationwide due to reports of 15mm connector disconnection. The defect could affect ventilation during use.
Teleflex is recalling over 1 million Flexi-Set Cuffed Endotracheal Tube kits due to reports of 15mm connector disconnection from the tube. The recall affects products distributed nationwide.
TELEFLEX endotracheal tubes are being recalled due to reports of the 15mm connector disconnecting from the tube. The recall affects 860,472 units distributed nationwide, including Puerto Rico.
Teleflex is recalling 35,513 preformed AGT oral endotracheal tubes nationwide due to reported connector disconnection from the 15mm tube connector.
Teleflex is recalling Preformed AGT Oral Endotracheal Tubes due to reports that the 15mm connector may disconnect from the tube. The recall affects 5,120 units distributed nationwide.
Teleflex LLC recalls 14,780 preformed AGT oral endotracheal tubes due to reports of 15mm connector disconnection. Units were distributed nationwide.
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.
Teleflex is recalling approximately 10,600 Flexi-Set Uncuffed Endotracheal Tube and Stylet Sets due to reports that the 15mm connector may disconnect from the tube during use.
Teleflex is recalling Slick Set Cuffed Endotracheal Tube and Stylet Sets due to reports of disconnection of the 15mm connector from the endotracheal tube. The affected units were distributed nationwide.
TELEFLEX LLC is recalling Flexi-Set Cuffed Endotracheal Tube and Stylet Sets nationwide due to reports of the 15mm connector disconnecting from the tube, posing a serious risk in critical care settings.
TELEFLEX is recalling Slick Set Cuffed Endotracheal Tube and Stylet Sets due to reports that the 15mm connector may disconnect from the tube during use.
Teleflex is recalling approximately 2,550 Slick Set Uncuffed Endotracheal Tubes (REF 150020) due to reports of 15mm connector disconnection.
Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.
Teleflex
American medical device company
Source: Wikidata (Q7696143), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.