Teleflex recalls Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 170145) 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 170145) because reports indicate the 15mm connector may 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 may become disconnected during use, potentially causing breathing difficulties for patients. This disconnection could occur if the tube is moved or handled improperly during medical procedures.
Healthcare professionals using the affected endotracheal tubes during medical procedures are most at risk. Patients receiving intubation with these tubes could experience breathing issues if the connector disconnects.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set' with the reference number REF 170145. Affected units have specific batch numbers listed in the recall notice.
Review the product's UDI/DI code (14026704644923) and batch numbers (e.g., 18JG14, 19BG12) to confirm if your item is affected.
Reports indicate the 15mm connector may disconnect from the endotracheal tube, potentially causing breathing difficulties during medical procedures.
Check for the reference number REF 170145 and specific batch numbers listed in the recall notice (e.g., 18JG14, 19BG12).
The recall indicates a low risk of disconnection, so immediate action is not required. Check the product details to confirm if your item is affected.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1842-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1842-2023 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.
