Teleflex recalls Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 170140) due to reports of 15mm connector disconnection. Affected units have specific batch numbers and UDI/DI codes. Stop using if you own this medical device.
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 products (REF 170140) because reports indicate the 15mm connector can disconnect from the tube. This could lead to medical complications during procedures if the tube becomes disconnected.
The 15mm connector on the endotracheal tube can become disconnected from the tube during use, potentially causing airway interruption. This could lead to breathing difficulties or medical emergencies if the tube is not properly secured.
Healthcare professionals and medical facilities that use these endotracheal tubes for intubation procedures. Patients undergoing surgery or medical treatments requiring airway management are at risk if the tube disconnects during use.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set' with reference number REF 170140. Look for batch numbers listed in the record: 18JG17, 18JG32, 18JG34, 18KG29, 18LG02, 18LG15, 18LG18, 19AG09, 19AG21, 19BG12, 19CT32, 19DT06, 19DT20, 19ET38, 19ET72, 19ET77, 19FT24, 19JT29, 20BG16, 20CT36, 20DT37, 20ET28, 20GG45, 20GT14, KME20H2017, KME20K0772, KME20K2549, KME20K2584, KME20L1491, KME20L2402, KME21A1159, KME21A1900, KME21A2810, KME21B0572, KME21B1688, KME21C0024, KME21C0493, KME21C2999, KME21L1921, KME21L1922, KME22B1077, KME22C2262, KME22C3452, KME22E1239, KME22F0049, KME22F1951, KME22H0913, KME22H0967, KME22H2910.
Identify if your tube has the reference number REF 170140 and the listed batch numbers or UDI/DI codes.
If you have the recalled product, stop using it immediately to prevent potential disconnection during medical procedures.
The recalled product is the Slick Set Uncuffed Endotracheal Tube and Stylet Set with reference number REF 170140.
Check for the reference number REF 170140 and the specific batch numbers listed in the recall record, such as 18JG17, 18JG32, or KME20H2017.
The recall record does not specify a return process, 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-1841-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1841-2023 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.
