Teleflex recalls Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 150025) 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 150025) 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 endotracheal tube can become disconnected during use, potentially causing breathing difficulties. This disconnection may occur if the tube is moved or handled improperly, especially in critical care settings.
Healthcare professionals using the affected endotracheal tubes during medical procedures are most at risk. Patients receiving anesthesia or critical care may be impacted if the tube disconnects.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set' with reference number 150025. Affected units have batch numbers 18GT32, 18HG07, 18HG16, 18HG29, 18HG38, 18IG06, 18IG17, 18IG21, or 18IG27 and UDI/DI code 4026704319657.
Inspect the 15mm connector on the endotracheal tube for signs of disconnection or damage.
Teleflex is recalling these endotracheal tubes due to reports of the 15mm connector disconnecting from the tube during use.
Check the batch numbers and UDI/DI code on the product to see if it's affected. If it is, stop using it and contact Teleflex for further instructions.
The recall reports disconnection, which could cause breathing difficulties during medical procedures, but the record does not specify if this leads to serious injury.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1901-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1901-2023 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.
