Teleflex recalls Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 170135) 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 Uncuffed Endotracheal Tube and Stylet Set products (REF 170135) 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 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 connections are critical.
Healthcare professionals using these tubes during medical procedures are most at risk. Patients receiving care with the recalled products could experience breathing issues if the tube disconnects.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set' with the reference number REF 170135. Affected units have specific batch numbers listed in the recall notice, including UDI/DI codes starting with 14026704647030.
Review the product's reference number (REF 170135) and batch numbers listed in the recall notice to confirm if your item is affected.
If you are a healthcare professional using this product, contact your medical facility to determine if the affected batch numbers are in use and follow their instructions for replacement.
This product is intended for medical use only and is not designed for home use. Healthcare professionals should follow the recall instructions.
If you are a healthcare professional using this product, contact your medical facility to determine if the affected batch numbers are in use and follow their instructions for replacement.
Check for the reference number REF 170135 and the specific batch numbers listed in the recall notice, including UDI/DI codes starting with 14026704647030.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1840-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1840-2023 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.
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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.
