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 can 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 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 potential medical emergencies.
Healthcare professionals using the recalled endotracheal tubes during medical procedures are most at risk. Patients receiving these tubes could experience breathing difficulties if the connector disconnects.
Check for the batch numbers listed: 18FG12, 18FG23, 18GG03, 18GT26, 18HG24, 18JG14, 18KG08, 18KG22, 18LG31, 19AG09, 19AG11, 19AG21, 19DT42, 19ET34, 19FT18, 19GT44, 19HT66, 19JT01, 19JT20, 19KT17, 19LT04, 19LT08, 19LT31, 19LT32, 20AT09, 20CT23, 20DT29, KME20L1712, KME20M0352. The product has a unique identifier (UDI/DI) of 14026704341082.
Look for the batch numbers listed in the recall notice: 18FG12, 18FG23, 18GG03, 18GT26, 18HG24, 18JG14, 18KG08, 18KG22, 18LG31, 19AG09, 19AG11, 19AG21, 19DT42, 19ET34, 19FT18, 19GT44, 19HT66, 19JT01, 19JT20, 19KT17, 19LT04, 19LT08, 19LT31, 19LT32, 20AT09, 20CT23, 20DT29, KME20L1712, KME20M0352.
If you have the recalled tube, contact Teleflex directly to arrange for a replacement or other remedy.
The affected batch numbers are: 18FG12, 18FG23, 18GG03, 18GT26, 18HG24, 18JG14, 18KG08, 18KG22, 18LG31, 19AG09, 19AG11, 19AG21, 19DT42, 19ET34, 19FT18, 19GT44, 19HT66, 19JT01, 19JT20, 19KT17, 19LT04, 19LT08, 19LT31, 19LT32, 20AT09, 20CT23, 20DT29, KME20L1712, KME20M0352.
Check the batch numbers on your tube against the list provided in the recall notice: 18FG12, 18FG23, 18GG03, 18GT26, 18HG24, 18JG14, 18KG08, 18KG22, 18LG31, 19AG09, 19AG11, 19AG21, 19DT42, 19ET34, 19FT18, 19GT44, 19HT66, 19JT01, 19JT20, 19KT17, 19LT04, 19LT08, 19LT31, 19LT32, 20AT09, 20CT23, 20DT29, KME20L1712, KME20M0352.
If you have the recalled tube, contact Teleflex directly to arrange for a replacement or other remedy.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1945-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1945-2023 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.
