Teleflex recalls specific endotracheal tube models due to reported disconnections. Affected units have unique batch numbers and UDI/DI codes. Consumers should stop using and contact Teleflex for details.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling certain endotracheal tubes because they can disconnect from the tube. This risk could lead to breathing problems during medical procedures if the tube becomes disconnected.
The 15mm connector can disconnect from the endotracheal tube during use. This disconnection could cause breathing difficulties or require immediate medical intervention if the tube becomes separated.
Healthcare professionals using these tubes in medical settings are most at risk. Patients receiving intubation care with the affected models may also be impacted.
Check for batch numbers listed: 18FG07, 18JG33, 18JG36, 18LT16, 19CT26, 19KT38, 19LT07, 20AT41, 20CT13, 20ET17, KME20K1512, KME22B0593, KME22E2347, KME22H1178, KME22H3021. Also look for the UDI/DI code 14026704341266.
Identify the batch numbers and UDI/DI code on your endotracheal tube to confirm if it's affected.
Reach out to Teleflex directly for further instructions on how to proceed with the recall.
Teleflex reports disconnections of the 15mm connector from the endotracheal tube for these specific models.
Check for batch numbers: 18FG07, 18JG33, 18JG36, 18LT16, 19CT26, 19KT38, 19LT07, 20AT41, 20CT13, 20ET17, KME20K1512, KME22B0593, KME22E2347, KME22H1178, KME22H3021. Also look for the UDI/DI code 14026704341266.
Contact Teleflex directly for instructions on how to handle the affected product.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1958-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1958-2023 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.
