Teleflex recalls specific endotracheal tubes due to reported disconnection of 15mm connectors. Affected models 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 endotracheal tubes because reports show 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 endotracheal tubes can disconnect during use. This disconnection could cause breathing problems for patients if the tube becomes separated from the ventilator or breathing apparatus.
Healthcare professionals using the recalled endotracheal tubes for medical procedures are most at risk. Patients receiving these tubes during surgery or critical care may be affected.
Check for batch numbers listed: 18FG02, 18GG15, 18IG13, 18IG22, 18JG17, 18JG38, 19BG21, 19DT19, 19GT24, 19HT26, 19JT20, 19KT19, 19KT38, 19KT50, 19LT46, 19LT47, 20AT06, 20BT09, 20DT23, 20GG39, KME21G0866, KME22A2268, KME22B0062.
Inspect the 15mm connector on the endotracheal tube for signs of disconnection or damage.
The recall involves Teleflex Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff with reference number 112080080.
Check the batch numbers listed: 18FG02, 18GG15, 18IG13, 18IG22, 18JG17, 18JG38, 19BG21, 19DT19, 19GT24, 19HT26, 19JT20, 19KT19, 19KT38, 19KT50, 19LT46, 19LT47, 20AT06, 20BT09, 20DT23, 20GG39, KME21G0866, KME22A2268, KME22B0062.
The recall does not specify a remedy, so contact Teleflex directly for guidance on handling the affected tubes.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1963-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1963-2023 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.
