Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected units have unique batch numbers and UDI/DI codes. Consumers should check their product details.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling certain endotr: tubes that may disconnect at the 15mm connector. This could lead to breathing issues during medical procedures if the tube becomes disconnected.
The 15mm connector on these tubes can disconnect during use, potentially causing breathing difficulties. This disconnection risk is reported but not guaranteed to occur in every case.
Healthcare professionals and patients using these endotracheal tubes during medical procedures. Those with the specific batch numbers or UDI/DI codes listed are most at risk.
Check for the UDI/DI code 14026704341266 and batch numbers 18IT25, 18JG13, 19CT66, 19HT79, 19KT08, 20BT13, 20DT19, or KME22C0673 on the tube packaging.
Look for the UDI/DI code 14026704341266 and batch numbers listed in the recall notice.
Teleflex reports disconnections of the 15mm connector from the endotracheal tube, which could cause breathing issues during medical procedures.
Check for the UDI/DI code 14026704341266 and batch numbers 18IT25, 18JG13, 19CT66, 19HT79, 19KT08, 20BT13, 20DT19, or KME22C0673.
The recall does not specify a remedy, so contact Teleflex directly for guidance.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1882-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1882-2023 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.
