Teleflex recalls Slick Set Cuffed Endotracheal Tube and Stylet Set (REF 170080) due to reports of 15mm connector disconnection. Affected units have specific batch numbers and UDI/DI codes.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling Slick Set Cuffed Endotracheal Tube and Stylet Set products because reports indicate the 15mm connector can disconnect from the endotracheal tube. This could lead to breathing difficulties during medical procedures if the tube becomes disconnected.
The 15mm connector on the endotracheal tube can become disconnected during use, potentially causing breathing difficulties. This disconnection may occur if the tube is moved or handled improperly, especially in medical settings where precise positioning is critical.
Healthcare professionals using these tubes during medical procedures are most at risk. Patients receiving intubation care with the affected products could experience breathing issues if the tube disconnects.
Check for the product name 'Slick Set Cuffed Endotracheal Tube and Stylet Set' with reference number 170080. Affected units have specific batch numbers listed in the recall notice, including UDI/DI codes starting with 4026704319596.
Identify the product by checking the reference number (170080) and batch numbers listed in the recall notice.
If you use this product, contact your healthcare provider to determine if you have an affected unit and whether immediate action is needed.
Teleflex recalls these products due to reports of the 15mm connector disconnecting from the endotracheal tube, which could cause breathing difficulties during medical procedures.
Affected batch numbers include 18FG09, 18FG20, 18FT32, and other specific codes listed in the recall notice.
Check for the reference number 170080 and the specific batch numbers or UDI/DI codes starting with 4026704319596 as listed in the recall notice.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1833-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1833-2023 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.
