Teleflex recalls specific Preformed AGT Oral Endotracheal Tubes due to reported disconnection of the 15mm connector. Affected units have unique batch numbers and reference codes. Consumers should check their product details to determine if recalled.
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 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 unplugged from the patient's airway, leading to breathing difficulties or medical emergencies.
Healthcare professionals using the affected tubes during medical procedures are most at risk. Patients receiving these tubes may experience breathing issues if the connector disconnects.
Check for the reference code 100180055 and batch numbers listed in the recall notice: 18IG24, 18JG36, 18LG33, 19AG11, 19AG21, 19DT06, 19ET58, 19FT22, 19FT49, 19HT04, 19HT34, 19HT80, 19IT43, 19JT02, 20AT49, 20BT53, 20CT24, 20DT24, 20GG27, KME20K2673, KME20M0950, KME21A0310, KME21B0602, KME22F0738.
Identify your tube's reference code and batch numbers to see if it matches the recalled items listed in the notice.
Teleflex is recalling these tubes because reports indicate the 15mm connector can disconnect during use, potentially causing breathing difficulties.
Check for the reference code 100180055 and batch numbers listed in the recall notice: 18IG24, 18JG36, 18LG33, 19AG11, 19AG21, 19DT06, 19ET58, 19FT22, 19FT49, 19HT04, 19HT34, 19HT80, 19IT43, 19JT02, 20AT49, 20BT53, 20CT24, 20DT24, 20GG27, KME20K2673, KME20M0950, KME21A0310, KME21B0602, KME22F0738.
The recall does not specify a remedy, so you should contact Teleflex directly to determine next steps.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1866-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1866-2023 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.
