Teleflex recalls Slick Set Cuffed Endotracheal Tube and Stylet Set (REF 170070) due to reported disconnections at the 15mm connector. Affected units have specific batch numbers and UDI/DI codes. Consumers should check their product details.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling Slick Set Cuffed Endotracheal Tube and Stylet Set products (REF 170070) because reports indicate the 15mm connector can disconnect from the endotracheal tube. This could lead to breathing issues during medical procedures if the tube becomes disconnected.
The 15mm connector on the endotracheal tube can disconnect during use, potentially causing breathing difficulties for patients. This disconnection risk occurs when the tube is attached to the patient's airway system.
Healthcare professionals and medical facilities using the affected Slick Set Cuffed Endotracheal Tube and Stylet Set products for patient airways. Those with the specific batch numbers or UDI/DI codes listed are most at risk.
Check for the product name 'Slick Set Cuffed Endotracheal Tube and Stylet Set' with reference number REF 170070. Affected units have specific batch numbers listed in the recall notice or UDI/DI code 4026704319572.
Look for the reference number REF 170070 and the UDI/DI code 4026704319572 on the product packaging or label.
Teleflex reports that the 15mm connector can disconnect from the endotracheal tube, which may cause breathing issues during medical procedures.
Affected batch numbers include 18FG09, 18FG15, 18FG17, and many others as listed in the recall notice.
The recall does not require immediate discontinuation; healthcare professionals should check product details and follow the provided steps to ensure safety.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1831-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1831-2023 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.
