Teleflex recalls Flexi-Set Cuffed Endotracheal Tube and Stylet Set (REF 504570) due to reports of 15mm connector disconnection. Affected units have specific batch numbers and UDI/DI codes.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling Flexi-Set Cuffed Endotracheal Tube and Stylet Set products (REF 504570) because reports indicate the 15mm connector can disconnect from the endotracheal tube. This could lead to breathing difficulties during medical procedures.
The 15mm connector on the endotracheal tube can become disconnected during use, potentially causing breathing difficulties for patients. This disconnection may occur during medical procedures when the tube is being handled or moved.
Healthcare professionals using the affected endotracheal tubes for intubation procedures are most at risk. Patients receiving these tubes during medical treatment could experience breathing issues if the connector disconnects.
Check for the product name 'Flexi-Set Cuffed Endotracheal Tube and Stylet Set' with reference number 504570. Affected units have specific batch numbers listed in the recall notice or UDI/DI code 4026704547616.
Look for the reference number 504570 and batch numbers listed in the recall notice or UDI/DI code 4026704547616.
The recall reports disconnections of the 15mm connector from the endotracheal tube, which could cause breathing difficulties during medical procedures. However, no injuries have been reported.
Check for the reference number 504570 and batch numbers listed in the recall notice or UDI/DI code 4026704547616.
The recall does not specify a remedy, so contact Teleflex directly for guidance on handling the product.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1849-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1849-2023 from Teleflex. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
