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 may 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 can become disconnected during use, potentially causing breathing difficulties or requiring immediate medical intervention. This disconnection risk is specific to the design of the connector in the recalled models.
Healthcare professionals and medical facilities using the affected endotracheal tubes. Patients receiving intubation procedures are at risk if the tube disconnects during critical medical care.
Check for the unique batch numbers listed in the recall notice (e.g., 18FT39, 18GT32) or the UDI/DI code 14026704341204 on the tube packaging. The product name is Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff.
Look for the unique batch numbers (e.g., 18FT39) or UDI/DI code 14026704341204 on the tube packaging to confirm if your product is affected.
Reach out to Teleflex customer support for assistance with the recall and to determine if your specific model is affected.
Reports indicate the 15mm connector may disconnect from the endotracheal tube, potentially causing breathing difficulties during medical procedures.
Check for the unique batch numbers listed in the recall (e.g., 18FT39) or the UDI/DI code 14026704341204 on the tube packaging.
Contact Teleflex customer support to determine if your specific model is affected and follow their instructions for next steps.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1954-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1954-2023 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.
