Teleflex recalls specific 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.
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 issues during medical procedures if the tube becomes disconnected.
The 15mm connector on the affected tubes has reportedly disconnected during use. This disconnection could cause the tube to become unplugged from the patient's airway, potentially leading to breathing difficulties or medical emergencies.
Healthcare professionals and medical facilities using the affected Preformed AGT Oral Endotracheal Tubes are most at risk. Patients receiving these tubes during procedures may experience breathing difficulties if disconnection occurs.
Check for the unique batch numbers listed in the recall notice (e.g., 18GG18, 19BG18) or the UDI/DI code 14026704341242 on the tube packaging. The affected tubes are identified by the specific model and reference numbers provided in the recall.
Look for the unique batch numbers (e.g., 18GG18, 19BG18) or UDI/DI code 14026704341242 on the tube packaging to confirm if your product is affected.
Teleflex is recalling these tubes due to reports of the 15mm connector disconnecting from the endotracheal tube, which could cause breathing issues during medical procedures.
Check for the unique batch numbers listed in the recall notice (e.g., 18GG18, 19BG18) or the UDI/DI code 14026704341242 on the tube packaging.
The recall does not specify a remedy, so contact Teleflex directly to determine next steps for affected products.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1957-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1957-2023 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.
