Teleflex recalls Slick Set Uncuffed Endotracheal Tube and Stylet Set (REF 170155) due to reported disconnections of the 15mm connector. 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 products (REF 170155) because reports indicate the 15mm connector can disconnect from the endotracheal tube. This disconnection could lead to breathing difficulties during medical procedures.
The 15mm connector on the endotracheal tube can become disconnected during use, potentially causing breathing difficulties for patients. This disconnection may occur if the connector is not securely attached to the tube.
Healthcare professionals using the affected endotracheal tubes during medical procedures are most at risk. Patients receiving these tubes could experience breathing issues if the connector disconnects.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set' with the reference number REF 170155. Affected units have specific batch numbers listed in the recall notice.
Identify the product by checking the reference number REF 170155 and the batch numbers listed in the recall notice.
Teleflex recalls these products due to reports of the 15mm connector disconnecting from the endotracheal tube, which could cause breathing difficulties during medical procedures.
Affected batch numbers include 18JG17, 19AG37, 19CT32, 19ET22, 19ET38, 19ET60, 19IT54, 20AT32, 20CT22, 20DT29, KME20G0385, KME20K2550, KME20L1492, KME20M0813, KME21A2775, KME21B1698, KME21C2646, KME21J0882, KME21J0883, KME22F0239, KME22F0718, KME22F2420, KME22J0254, KME22J0262, KME22K2780.
Check for the product name 'Slick Set Uncuffed Endotracheal Tube and Stylet Set' with reference number REF 170155 and the specific batch numbers listed in the recall notice.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1844-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1844-2023 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.
