Teleflex recalls Flexi-Set Cuffed Endotracheal Tube and Stylet Set (REF 504580) due to reports of 15mm connector disconnection. Affected units have specific batch numbers and UDI/DI codes. Consumers should check their product details.
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 504580) 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 disconnect during use, which may cause breathing difficulties or require immediate medical intervention. This disconnection risk is reported in healthcare settings where the tubes are used for airway management.
Healthcare professionals and medical facilities using the Flexi-Set Cuffed Endotracheal Tube and Stylet Set (REF 504580) with the listed batch numbers and UDI/DI codes are most at risk. Patients receiving these tubes during medical procedures could be affected if disconnection occurs.
Check for the product name 'Flexi-Set Cuffed Endotracheal Tube and Stylet Set' with the reference number REF 504580. Affected units have specific batch numbers listed in the recall notice and UDI/DI code 4026704547630.
Identify the product by checking the reference number REF 504580 and UDI/DI code 4026704547630 on the item.
Teleflex is recalling these products due to reports of the 15mm connector disconnecting from the endotracheal tube, which could cause breathing issues during medical procedures.
Check for the reference number REF 504580 and UDI/DI code 4026704547630 on the product. Affected units have specific batch numbers listed in the recall notice.
The recall does not specify a remedy, so contact Teleflex directly to determine next steps for affected products.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1851-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1851-2023 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.
