FDA (Devices) recall action 92373
The FDA (Devices) publishes a recall like this one as 123 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 123 pages.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
The agency’s own wording, quoted from the enforcement report.
The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.
Teleflex is recalling 20,042 endotracheal tubes due to reports of 15mm connector disconnection that could compromise airway management. The FDA classified this as a Class I recall.
TELEFLEX is recalling 5,600 endotracheal tubes nationwide due to reports of 15mm connector disconnection that could compromise airway management during patient care.
Teleflex is recalling 1,110 endotracheal tubes due to reports of 15mm connector disconnection. The affected units are distributed nationwide in the US and Puerto Rico.
Teleflex is recalling approximately 2,550 Slick Set Uncuffed Endotracheal Tubes (REF 150020) due to reports of 15mm connector disconnection.
The FDA is recalling approximately 302,652 Teleflex preformed oral endotracheal tubes nationwide due to reports of disconnection between the 15mm connector and the tube. Healthcare providers should immediately discontinue use of affected units.
TELEFLEX LLC is recalling Preformed AGT Oral Endotracheal Tubes because the 15mm connector may disconnect from the tube, creating a potential airway access risk.
Teleflex is recalling 31,945 RUSCHELIT Safety Clear Tracheal Tubes nationwide due to reports of 15mm connector disconnection from the endotracheal tube.
Teleflex is recalling 8,610 Preformed AGT Oral Endotracheal Tubes nationwide due to reports that the 15mm connector can disconnect from the tube.
TELEFLEX is recalling 760 endotracheal tubes due to reports of 15mm connector disconnection. This medical device failure could compromise airway management during critical care.
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 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 LLC is recalling Slick Set Cuffed Endotracheal Tube and Stylet Sets due to reports of the 15mm connector disconnecting from the tube. Approximately 4,370 units distributed nationwide including Puerto Rico are affected.
TELEFLEX LLC recalls RUSCHELIT Safety Clear Tracheal Tubes due to reports of 15mm connector disconnection. The Class I recall affects 30,391 units distributed nationwide including Puerto Rico.
TELEFLEX is recalling approximately 8,620 Preformed AGT Oral Endotracheal Tubes distributed nationwide due to reports of disconnection of the 15mm connector from the tube.
Teleflex is recalling 14,480 Preformed AGT Oral Endotracheal Tubes nationwide due to reports of 15mm connector disconnection 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 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 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 (Murphy design) may have a disconnected 15mm connector. Approximately 12,382 affected units were distributed nationwide. Healthcare facilities should inspect tubes before use.
Teleflex LLC recalls 14,780 preformed AGT oral endotracheal tubes due to reports of 15mm connector disconnection. Units were distributed nationwide.
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 18,620 endotracheal tubes due to reported disconnection of 15mm connectors. The tubes are used for oral and nasal intubation and were distributed nationwide.
Teleflex is recalling approximately 446,163 Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection. The connector failure could affect tube function during patient airway management.
Teleflex is recalling endotracheal tubes due to reports of disconnection between the tube and its 15mm connector. Affected devices were distributed nationwide including Puerto Rico.
Teleflex is recalling endotracheal tubes due to reports of 15mm connector disconnection. The FDA Class I recall affects approximately 30,423 units distributed nationwide.