Teleflex recalls Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 150030) due to reported disconnection of 15mm connectors. 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 150030) because reports show 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 disconnect during use, potentially causing breathing difficulties. This disconnection risk occurs when the tube is being handled or moved, especially in medical settings where precise connections are critical.
Healthcare professionals using the affected endotracheal tubes during medical procedures are most at risk. Patients receiving care with these tubes could experience breathing issues if disconnected.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set' with reference number REF 150030. Affected units have batch numbers 18IG15, 18IG21, 18IG27, 18JG02, or 18JG14 and UDI/DI code 4026704319664.
Inspect the 15mm connector on the endotracheal tube for signs of disconnection or looseness.
Teleflex is recalling these tubes due to reports of the 15mm connector disconnecting from the endotracheal tube, which could cause breathing difficulties during medical procedures.
Affected batch numbers are 18IG15, 18IG21, 18IG27, 18JG02, and 18JG14.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set' with reference number REF 150030 and the UDI/DI code 4026704319664.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1902-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1902-2023 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.
