Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected models include REF 112082085 with listed batch numbers. 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 endotracheal tubes that have reported disconnections at the 15mm connector. This could lead to breathing issues during medical procedures if the tube becomes disconnected.
The 15mm connector on the affected tubes can disconnect during use, potentially causing breathing difficulties. This disconnection risk occurs when the tube is attached to medical equipment or during patient procedures.
Healthcare professionals and medical facilities using the recalled endotracheal tubes are most at risk. Patients receiving these tubes during procedures may face breathing complications if disconnected.
Check for the product reference number REF 112082085 and batch numbers listed in the recall notice. The specific batch numbers include 18HG37 through 20ET17 and other codes starting with KME20.
Review the product reference number and batch numbers to confirm if your tube is affected.
Teleflex reports disconnections of the 15mm connector on these specific endotracheal tubes, which could cause breathing issues during medical procedures.
Check for the product reference number REF 112082085 and batch numbers listed in the recall notice, including codes starting with 18HG37 through 20ET17 and KME20.
The recall does not specify a remedy, so contact Teleflex directly for guidance on next steps.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1891-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1891-2023 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.
