Teleflex recalls Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 150055) due to reported disconnections. 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 a specific type of endotracheal tube and stylet set 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 risk occurs during medical procedures when the tube is in place.
Healthcare professionals using the affected endotracheal tube sets for medical procedures are most at risk. Patients receiving these tubes during surgery or critical care may be affected if the tube disconnects.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set' with reference number 150055. Affected units have UDI/DI code 4026704319718 and batch number 18FG05.
Verify the product name, reference number 150055, UDI/DI code 4026704319718, and batch number 18FG05 to confirm if your item is affected.
Teleflex reports disconnections of the 15mm connector from the endotracheal tube for these specific products.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set' with reference number 150055, UDI/DI code 4026704319718, and batch number 18FG05.
The recall record does not specify a remedy, so contact Teleflex directly for guidance.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1905-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1905-2023 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.
