Teleflex recalls specific models of Preformed AGT Oral Endotracheal Tubes due to reports of 15mm connector disconnection. Affected units have batch numbers listed in the recall notice.
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 with a risk of the 15mm connector disconnecting. This could lead to breathing issues during medical procedures if the tube becomes disconnected.
The 15mm connector on the affected tubes can disconnect during use, potentially causing breathing difficulties for patients. This disconnection risk is reported but not yet confirmed to cause injuries.
Healthcare professionals using these endotracheal tubes in medical settings are most at risk. Patients undergoing procedures with these tubes may face breathing complications if disconnection occurs.
Check for batch numbers listed in the recall: 18FG33 through KME22H1202. The product name is Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781045.
Inspect the 15mm connector on the tube for signs of disconnection or damage.
The recall reports disconnections but has not confirmed injuries. Users should check for connector issues.
Look for batch numbers listed in the recall: 18FG33 through KME22H1202. The product name is Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781045.
The recall does not specify a stop-use action. Users should check for disconnection risks but no immediate stop is required.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1879-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1879-2023 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.
