Teleflex recalls Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 170130) 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 170130) 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 these tubes during surgery or critical care may experience breathing issues if the connector disconnects.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set' with reference number REF 170130. Affected units have specific batch numbers listed in the recall notice, including UDI/DI codes starting with 14026704644893.
Look for the reference number REF 170130 and UDI/DI code 14026704644893 on the product packaging.
Reach out to Teleflex customer service for assistance with the recall and to confirm if your product is affected.
Reports indicate the 15mm connector can disconnect from the endotracheal tube, potentially causing breathing difficulties during medical procedures.
Check for the reference number REF 170130 and UDI/DI code 14026704644893. Affected units have specific batch numbers listed in the recall notice.
Contact Teleflex customer service to confirm if your product is affected and follow their instructions 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-1839-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1839-2023 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.
