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 recalled.
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, potentially causing the tube to become dislodged from the patient's airway. This could lead to breathing difficulties or the need for emergency re-intubation.
Healthcare professionals using the affected endotracheal tubes during medical procedures are most at risk. Patients receiving these tubes could experience breathing issues if the connector disconnects.
Check for the product name 'Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff' with the specific reference number 111780075. Affected units have batch numbers listed in the record, including 18FG21 through 20ET49 and other codes.
Identify if your tube has the reference number 111780075 and the listed batch numbers or UDI/DI codes.
Teleflex is recalling these tubes after reports of the 15mm connector disconnecting from the tube, which could cause breathing difficulties during medical procedures.
Check for the reference number 111780075 and batch numbers listed in the record, including 18FG21 through 20ET49 and other codes.
The recall does not specify a remedy, so contact Teleflex directly to determine if your tube is affected and what steps to take.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1877-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1877-2023 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.
