Teleflex recalls Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 170120) 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 170120) 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 due to normal handling or movement during medical procedures.
Healthcare professionals using these tubes during medical procedures are most at risk. Patients receiving care with the affected products could experience breathing issues if the tube disconnects.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set' with reference number REF 170120. Affected units have specific batch numbers listed in the recall notice or UDI/DI code 14026704644879.
Look for the reference number REF 170120 and the UDI/DI code 14026704644879 on the product packaging.
Reach out to Teleflex customer service for assistance with the recall and to confirm if your product is affected.
Teleflex is recalling these products due to reports of the 15mm connector disconnecting from the endotracheal tube, which could cause breathing difficulties during medical procedures.
Healthcare providers should check if their equipment has the reference number REF 170120 and the UDI/DI code 14026704644879, then contact Teleflex for guidance.
The recall addresses a potential risk of breathing difficulties if the tube disconnects during use, but no specific incidents have been reported causing harm.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1837-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1837-2023 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.
