Teleflex recalls Flexi-Set Uncuffed Endotracheal Tube and Stylet Set (REF 506535) 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 Flexi-Set Uncuffed Endotracheal Tubes and Stylet Sets that have reported disconnection of the 15mm connector. 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 may occur if the tube is moved or handled improperly during medical procedures.
Healthcare professionals using these tubes during medical procedures are most at risk. Patients receiving care with the affected products could experience breathing issues if the tube disconnects.
Check for the product name 'Flexi-Set Uncuffed Endotracheal Tube and Stylet Set' with reference number 506535. Affected units have specific batch numbers and UDI/DI codes listed in the recall notice.
Look for the reference number 506535 and specific batch numbers or UDI/DI codes listed in the recall notice.
If you have the affected product, contact your healthcare provider for guidance on next steps.
The recalled product is Flexi-Set Uncuffed Endotracheal Tube and Stylet Set with reference number 506535.
Check for the reference number 506535 and specific batch numbers or UDI/DI codes listed in the recall notice.
The recall does not specify an immediate stop-use requirement; healthcare providers should be contacted 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-1856-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1856-2023 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.
