Teleflex recalls Flexi-Set Uncuffed Endotracheal Tube and Stylet Set (REF 506540) 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 Tube and Stylet Set products that have reported issues with the 15mm connector disconnecting from the tube. This could lead to breathing difficulties during medical procedures if the tube becomes disconnected.
The 15mm connector on the endotracheal tube can become disconnected during use, potentially causing breathing difficulties for patients. This disconnection may occur during medical procedures when the tube is being handled or moved.
Healthcare professionals using these 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 'Flexi-Set Uncuffed Endotracheal Tube and Stylet Set' with reference number 506540. Affected units have specific batch numbers and UDI/DI codes listed in the recall notice.
Look for the reference number 506540 and batch numbers listed in the recall notice to confirm if your product is affected.
The recall reports disconnections but does not indicate that the product is dangerous when used correctly.
Check for the reference number 506540 and specific batch numbers or UDI/DI codes listed in the recall notice.
The recall does not specify a remedy, so contact Teleflex directly for guidance on next steps.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1857-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1857-2023 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.
