Teleflex recalls Slick Set Cuffed Endotracheal Tube and Stylet Set (REF 170060) 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 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 for patients. This disconnection may occur during medical procedures when the tube is being handled or moved.
Healthcare professionals using the affected endotracheal tubes during medical procedures are most at risk. Patients receiving these tubes could experience breathing issues if disconnected.
Check for the product name 'Slick Set Cuffed Endotracheal Tube and Stylet Set' with reference number REF 170060. Affected units have specific batch numbers listed in the recall notice or UDI/DI code 4026704319558.
Inspect the 15mm connector on the endotracheal tube for signs of disconnection or looseness.
Reach out to Teleflex directly for assistance with the recall if you own the affected product.
Teleflex reports that the 15mm connector can disconnect from the endotracheal tube, potentially causing breathing difficulties during medical procedures.
Affected batch numbers include 18GG31, 18HG22, 18HG32, 18HG35, 18IG09, 18IG24, 18IG27, 18JG17, 18LG12, 19AG37, 19BG12, 19CT49, 19DT15, 19DT20, 19ET22, 19ET38, 19ET77, 19FT18, 19IT14, 19IT25, 19JT42, 20DT29, 20ET04, 20FT34, 20FT54, 20GG41, and others listed in the recall notice.
Check for the product name 'Slick Set Cuffed Endotracheal Tube and Stylet Set' with reference number REF 170060. Affected units have specific batch numbers or UDI/DI code 4026704319558.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1829-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1829-2023 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.
