Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected products include certain batch numbers and model references. Consumers should check their product details and contact Teleflex for guidance.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling specific oral endotracheal tubes because reports indicate the 15mm connector can 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 may occur if the tube is moved or handled improperly, especially in medical settings where precise tube placement is critical.
Healthcare professionals and patients using these endotracheal tubes during medical procedures. Those with the specific batch numbers listed in the recall are most at risk.
Check the product label for the model reference number 111780070 and batch numbers listed in the recall. The unique device identifier (UDI/DI) 14026704341105 is also associated with these affected tubes.
Look for the model reference number 111780070 and batch numbers listed in the recall on the tube's label.
Reach out to Teleflex for further guidance on whether your tube is affected and what steps to take.
Teleflex is recalling these tubes due to reports of the 15mm connector disconnecting from the endotracheal tube, which could cause breathing difficulties during medical procedures.
Check the tube's label for the model reference number 111780070 and batch numbers listed in the recall, including the unique device identifier (UDI/DI) 14026704341105.
Contact Teleflex directly to determine if your tube is affected and follow their guidance for 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-1947-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1947-2023 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.
