Teleflex recalls Flexi-Set Uncuffed Endotracheal Tube and Stylet Set (REF 506530) 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 certain Flexi-Set Uncuffed Endotracheal Tube and Stylet Sets because reports indicate the 15mm connector can disconnect from the tube. This could lead to breathing issues during medical procedures if the tube becomes disconnected.
The 15mm connector on the endotracheal tube can become disconnected during use, potentially causing the tube to become dislodged from the patient's airway. This could lead to breathing difficulties or the need for emergency re-intubation.
Healthcare professionals using the affected endotracheal tubes for intubation procedures are most at risk. Patients undergoing surgery or medical treatments requiring these tubes may be affected if the device disconnects.
Check for the product name 'Flexi-Set Uncuffed Endotracheal Tube and Stylet Set' with the reference number 506530. Affected units have specific batch numbers and UDI/DI codes listed in the recall notice.
Identify the product by checking the reference number 506530 and the batch numbers listed in the recall notice.
Reach out to Teleflex for assistance with the recall process or to confirm if your specific unit is affected.
Reports indicate the 15mm connector can disconnect from the endotracheal tube, potentially causing breathing issues during medical procedures.
Check for the reference number 506530 and the specific batch numbers listed in the recall notice, which include codes like 18FG05 through KME22K0918.
The recall does not require immediate discontinuation; healthcare professionals should check product details and contact Teleflex 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-1855-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1855-2023 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.
