Teleflex recalls Flexi-Set Uncuffed Endotracheal Tube and Stylet Set (REF 506550) 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 Sets (REF 506550) 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 for patients. This disconnection could occur if the tube is moved or handled improperly during medical procedures.
Healthcare professionals using the affected endotracheal tubes during medical procedures are most at risk. Patients receiving these tubes during surgery or critical care may experience breathing issues if the connector disconnects.
Check for the product name 'Flexi-Set Uncuffed Endotracheal Tube and Stylet Set' with reference number 506550. Affected units have specific batch numbers listed in the recall notice, including UDI/DI code 4026704547715.
Look for the reference number 506550 and the UDI/DI code 4026704547715 on the product packaging.
The recall reports disconnections, but the product is safe if the connector remains securely attached. Healthcare providers should verify the product's status before use.
Check for the reference number 506550 and the UDI/DI code 4026704547715 on the product packaging. Affected units also have specific batch numbers listed in the recall notice.
The recall does not specify a remedy, so healthcare providers should check the product details and contact Teleflex for further guidance.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1859-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1859-2023 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.
