Teleflex recalls specific models of uncuffed 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 uncuffed 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 can become disconnected during use, potentially causing breathing difficulties for patients. This disconnection could occur during medical procedures if the tube is not properly secured.
Healthcare professionals and medical facilities using the affected Teleflex Preformed AGT Oral Endotracheal Tubes are most at risk. Patients receiving these tubes during procedures may face breathing issues if the connector disconnects.
Check the product label for the unique batch numbers listed: 18FG31, 18FT35, 18GG23, 18GT32, and other specific codes. The UDI/DI code 14026704340566 is also associated with these affected units.
Look for the unique batch numbers listed in the recall notice: 18FG31, 18FT35, 18GG23, 18GT32, and other specific codes.
Teleflex is recalling these tubes due to reports of the 15mm connector disconnecting from the tube, which could cause breathing difficulties during medical procedures.
Check the product label for the unique batch numbers listed: 18FG31, 18FT35, 18GG23, 18GT32, and other specific codes. The UDI/DI code 14026704340566 is also associated with these affected units.
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-1873-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1873-2023 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.
