Teleflex recalls Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 150020) 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 Tubes and Stylet Sets with a specific reference number because reports indicate the 15mm connector can disconnect from the tube. This could lead to medical complications during use.
The 15mm connector on the endotracheal tube can disconnect during use, potentially causing medical complications if the tube becomes dislodged. This issue is reported but not confirmed to cause serious injury in normal use.
Healthcare professionals using the affected endotracheal tubes and stylet sets are most at risk. Patients receiving these devices during medical procedures may be impacted.
Check for the reference number REF 150020 on the product. Affected units have specific batch numbers: 18FG01, 18FG05, 18HG07, 18HG22, 18HG27, 18HG38, 18IG02, 18JG04, 18JG06, 18JG17. The UDI/DI code 4026704319640 is also associated with these units.
Look for the reference number REF 150020 and the specific batch numbers listed in the recall notice.
Teleflex reports that the 15mm connector on the affected endotracheal tubes can disconnect, potentially causing medical complications.
Check for the reference number REF 150020 and batch numbers: 18FG01, 18FG05, 18HG07, 18HG22, 18HG27, 18HG38, 18IG02, 18JG04, 18JG06, 18JG17.
The recall notice does not specify a remedy, so contact Teleflex directly for further instructions.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1900-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1900-2023 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.
