Teleflex recalls specific endotracheal tubes due to reported disconnection of 15mm connectors. Affected models include REF 112080090 with batch numbers 18FT24, 18FT26, 19ET83, 19GT29, 19KT58, 19KT38.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling certain endotracheal tubes because reports indicate the 15mm connector may disconnect from the tube. This could lead to breathing difficulties during medical procedures if the tube becomes disconnected.
The 15mm connector on the endotracheal tube can disconnect during use, potentially causing breathing difficulties. This disconnection could lead to serious complications if the tube becomes separated from the patient's airway.
Healthcare professionals using these endotracheal tubes for medical procedures are most at risk. Patients undergoing surgery or critical care who receive these tubes may be affected.
Check for the model reference number REF 112080090 with batch numbers 18FT24, 18FT26, 19ET83, 19GT29, 19KT58, or 19KT38. These tubes were sold with the UDI/DI 14026704341266.
Inspect the 15mm connector on the endotracheal tube for signs of disconnection or damage.
Teleflex reports that the 15mm connector on these endotracheal tubes may disconnect during use, potentially causing breathing difficulties.
Batch numbers 18FT24, 18FT26, 19ET83, 19GT29, 19KT58, and 19KT38 are affected.
Check for the model reference number REF 112080090 with the batch numbers listed above or the UDI/DI 14026704341266.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1965-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1965-2023 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.