Teleflex recalls specific models of Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection. Affected units have unique batch numbers and UDI/DI codes. Consumers should check their product details to determine if they are affected.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling certain Preformed AGT Oral Endotracheal Tubes 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 affected tubes has been reported to disconnect during use. This disconnection could cause breathing difficulties or require immediate medical intervention if the tube becomes separated from the patient.
Healthcare professionals and patients using the recalled endotracheal tubes during medical procedures. Those with the specific batch numbers or UDI/DI codes listed are most at risk.
Check the product for batch numbers listed in the recall (e.g., 18FG12, 18FG24) or the unique device identifier (UDI/DI) code 14026704341068. The product name is Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff.
Identify your tube's batch number or UDI/DI code to see if it matches the listed affected units.
Teleflex reports of disconnection of the 15mm connector from the endotracheal tube for the affected products.
Check the product's batch number or UDI/DI code to determine if it is affected. If it is, contact Teleflex for further instructions.
Yes, disconnection could cause breathing difficulties during medical procedures, requiring immediate medical attention.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1943-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1943-2023 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.
