Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected models include REF 112082095 with certain batch numbers. Stop using if you have these items.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling endotracheal tubes with a specific model and batch numbers because reports show the 15mm connector can disconnect. This could lead to breathing problems during medical procedures if the tube becomes disconnected.
The 15mm connector on the endotracheal tube can disconnect during use, potentially causing breathing problems. This disconnection risk is reported in medical settings where the tube is critical for patient breathing.
Healthcare professionals and patients using these endotracheal tubes during medical procedures are most at risk. The affected products are used in critical care settings where disconnection could cause breathing issues.
Check for the model number REF 112082095 and batch numbers listed in the recall notice. The product is used in medical settings for breathing support during procedures.
Look for the model number REF 112082095 and batch numbers listed in the recall notice.
If you have the affected model and batch numbers, stop using the tube immediately as disconnection could cause breathing problems.
Reports of the 15mm connector disconnecting from the endotracheal tube during use.
Batch numbers include 18HG08, 18HT04, 18IG29, and others as listed in the recall notice.
The recall does not specify a return process, 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-1893-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1893-2023 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.
