Teleflex recalls Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 170125) 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 (REF 170125) 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 affected tubes has been reported to disconnect from the endotracheal tube. This disconnection could cause breathing difficulties during medical procedures, especially in critical care settings where continuous ventilation is required.
Healthcare professionals using the affected endotracheal tubes during medical procedures are most at risk. Patients receiving these tubes could experience breathing issues if the connector disconnects.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set' with reference number 170125. Affected units have specific batch numbers listed in the recall notice, including UDI/DI code 14026704644886.
Identify the product by checking the reference number (170125) and UDI/DI code (14026704644886) on the tube packaging.
Reach out to Teleflex directly for assistance with the recall if you have the affected product.
Reports indicate the 15mm connector can disconnect from the endotracheal tube, potentially causing breathing difficulties during medical procedures.
Check for the reference number 170125 and UDI/DI code 14026704644886 on the tube packaging. Affected units also have specific batch numbers listed in the recall notice.
Contact Teleflex directly for assistance with the recall if you have the affected product. The recall does not include a specific remedy like replacement or repair.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1838-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1838-2023 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.
