Teleflex recalls Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 150035) 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 150035) 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 is reported but not confirmed to cause injury in all cases.
Healthcare professionals using the affected endotracheal tubes for intubation procedures are most at risk. Patients receiving intubation care with these specific tubes may experience breathing issues if disconnection occurs.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set', reference number 150035, and batch numbers 18FG15, 18GG12, 18GG14, or 18JG02. The unique device identifier (UDI/DI) 4026704319671 is also associated with these units.
Verify the product name, reference number, batch numbers, and UDI/DI code to confirm if your item is affected.
The recall reports disconnections but does not state that injuries have occurred. The hazard is reported but not confirmed to cause serious injury.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set', reference number 150035, and batch numbers 18FG15, 18GG12, 18GG14, or 18JG02. The unique device identifier (UDI/DI) 4026704319671 is also associated with these units.
The recall does not specify a remedy, so the official notice does not provide instructions for action.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1903-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1903-2023 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.
