Teleflex recalls Flexi-Set Cuffed Endotracheal Tube and Stylet Set (REF 504575) 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 Set products (REF 504575) 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 become disconnected during use, potentially causing breathing difficulties for patients. This disconnection may occur due to improper handling or movement 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 difficulties if the tube disconnects.
Check for the product name 'Flexi-Set Cuffed Endotracheal Tube and Stylet Set' with reference number REF 504575. Affected units have specific batch numbers listed in the recall notice and unique device identifiers (UDI/DI) starting with 4026704547623.
Look for the reference number REF 504575 and batch numbers listed in the recall notice to confirm if your product is affected.
If you are a healthcare professional using this product, contact your institution to determine if your equipment is affected and follow their guidance.
Teleflex reports that the 15mm connector on the endotracheal tube can disconnect during use, potentially causing breathing issues for patients.
Check for the reference number REF 504575 and batch numbers listed in the recall notice, including unique device identifiers (UDI/DI) starting with 4026704547623.
If you are a healthcare professional using this product, contact your institution to determine if your equipment is affected and follow their guidance.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1850-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1850-2023 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.
