Teleflex recalls specific 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 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 has been reported to disconnect during use. This disconnection could cause the tube to become separated from the patient's airway, leading to breathing difficulties or the need for emergency intervention.
Healthcare professionals using these tubes during medical procedures are most at risk. Patients receiving these tubes during surgery or critical care may experience breathing issues if the connector disconnects.
Check the batch numbers on the tube: 18GG23, 18HG17, 18HG21, 18IG17, 18LG18, 19AG25, 19BG19, 19BG32, 19GT16, 19IT53, 19LT21, KME22F2174, KME22G1753. The product is a Preformed AGT Oral Endotracheal Tube uncuffed/plain model made by Teleflex.
Inspect the 15mm connector on the tube for signs of disconnection or damage.
Teleflex is recalling these tubes after reports of the 15mm connector disconnecting from the tube during use.
Affected batch numbers include 18GG23, 18HG17, 18HG21, 18IG17, 18LG18, 19AG25, 19BG19, 19BG32, 19GT16, 19IT53, 19LT21, KME22F2174, KME22G1753.
The recall does not require immediate stop use; however, healthcare professionals should check for disconnection before continuing use.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1870-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1870-2023 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.
