Teleflex recalls Flexi-Set Cuffed Endotracheal Tube and Stylet Set (REF 504550) 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 Cuffed Endotracheal Tube and Stylet Sets (REF 504550) because reports indicate the 15mm connector can disconnect 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. This disconnection could lead to complications if the tube is no longer properly secured to the patient's airway.
Healthcare professionals using these tubes for intubation procedures are most at risk. Patients undergoing surgery or medical treatments requiring endotracheal tubes may be affected if they use the recalled products.
Check for the product name 'Flexi-Set Cuffed Endotracheal Tube and Stylet Set' with reference number 504550. Affected units have specific batch numbers listed in the recall notice, including UDI/DI code 4026704547579.
Identify the product by checking the reference number (504550) and batch numbers listed in the recall notice.
Reports indicate the 15mm connector can disconnect from the endotracheal tube, potentially causing breathing difficulties during medical procedures.
Healthcare professionals using these tubes for intubation procedures are most at risk, as patients undergoing surgery or medical treatments requiring endotracheal tubes may be affected.
Check for the product name 'Flexi-Set Cuffed Endotracheal Tube and Stylet Set' with reference number 504550 and 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-1845-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1845-2023 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.
