Hazard
117 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 117 connector disconnection recalls we have scored against our rubric, 10 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 106 (91%) are Severe.
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all connector disconnection recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.
A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.
Teleflex is recalling 17,551 units of Flexi-Set Uncuffed Endotracheal Tubes nationwide after reports of the 15mm connector disconnecting from the tube.
TELEFLEX is recalling approximately 25,435 endotracheal tubes (REF 100382035) distributed nationwide due to reported disconnection of the 15mm connector from the device.
Teleflex is recalling 870 units of Slick Set Uncuffed Endotracheal Tubes nationwide due to reports of disconnection of the 15mm connector from the tube.
Teleflex LLC is recalling 19,842 preformed oral endotracheal tubes due to reports of 15mm connector disconnection. Affected devices were distributed nationwide.
Teleflex is recalling 190 endotracheal tubes due to reports of the 15mm connector disconnecting from the tube. This disconnection could compromise airway management and ventilation.
Teleflex LLC is recalling 7,800 endotracheal tubes due to reports of the 15mm connector disconnecting from the tube. The affected products were distributed nationwide in the US and Puerto Rico.
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.
Teleflex LLC is recalling Preformed AGT Oral Endotracheal Tubes due to reported connector disconnections. The recall affects 24,752 units distributed nationwide, including Puerto Rico.
TELEFLEX LLC is recalling RUSCHELIT Safety Clear Tracheal Tubes due to reports of 15mm connector disconnection. The recall involves 21,284 units distributed nationwide.
Teleflex LLC is recalling Slick Set Endotracheal Tube Sets for reports of 15mm connector disconnection. The connector may separate from the tube, affecting respiratory support in patients.
Teleflex is recalling 3,309 Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection. This defect may compromise airway management during medical use.
TELEFLEX is recalling 4,160 endotracheal tubes due to reports of the 15mm connector disconnecting from the tube. Affected units were distributed nationwide.
Teleflex is recalling Slick Set Cuffed Endotracheal Tubes due to reports of the 15mm connector disconnecting from the tube, which could interrupt airway support during mechanical ventilation.
TELEFLEX is recalling 5,990 endotracheal tubes due to reports of 15mm connector disconnection. Affected units were distributed nationwide, including Puerto Rico.
Teleflex is recalling 670 units of Preformed AGT Oral Endotracheal Tubes nationwide due to reports of 15mm connector disconnection from the tube.
TELEFLEX is recalling 16,570 units of Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection, which could compromise airway management during use.
TELEFLEX is recalling 2,382 Slick Set Uncuffed Endotracheal Tubes due to reports of 15mm connector disconnection. Units were distributed nationwide including Puerto Rico.
Teleflex recalls 53,216 Preformed AGT Endotracheal Tubes due to reported disconnection of the 15mm connector. Affected units were distributed nationwide including Puerto Rico.
TELEFLEX LLC is recalling 690 endotracheal tubes with high-volume, low-pressure cuff due to reports of connector disconnection. The affected products were distributed nationwide.
Teleflex is recalling RUSCHELIT Safety Clear Tracheal Tubes due to reports of 15mm connector disconnection. The affected tubes are distributed nationwide.
Teleflex is recalling Slick Set Cuffed Endotracheal Tubes because the 15mm connector may disconnect from the tube. The recall affects 1,460 units distributed nationwide, including Puerto Rico.
Teleflex LLC is recalling approximately 15,810 Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection. The affected units were distributed nationwide, including Puerto Rico.
Teleflex is recalling Slick Set endotracheal tubes due to reports of 15mm connector disconnection. The defect could prevent proper airway management during patient care.
Teleflex is recalling 4,146 preformed endotracheal tubes due to reports of 15mm connector disconnection. The affected devices were distributed nationwide.
Teleflex is recalling approximately 170,610 endotracheal tubes due to reports of 15mm connector disconnection. The disconnection could compromise airway management during mechanical ventilation.