Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected models include REF 112080085 with batch numbers 18IG19 to 20GT57. Consumers should check their product 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 reports indicate the 15mm connector can disconnect. This could lead to breathing difficulties during medical procedures if the tube becomes disconnected.
The 15mm connector on the affected endotracheal tubes has been reported to disconnect. This disconnection could cause breathing difficulties during medical procedures if the tube becomes disconnected.
Healthcare professionals and patients using the recalled endotracheal tubes are most at risk. The recall affects specific models used in medical settings.
Check for the model reference number REF 112080085 and batch numbers listed: 18IG19, 18KG26, 19CT61, 19GT31, 19JT19, 19KT38, 19LT17, 20CT02, 20DT23, 20ET17, 20GT57, KME22A1989.
Identify the model reference number and batch numbers listed in the recall notice to confirm if your tube is affected.
Teleflex reports of disconnection of the 15mm connector from the endotracheal tube for the affected products.
Check for the model reference number REF 112080085 and batch numbers listed: 18IG19, 18KG26, 19CT61, 19GT31, 19JT19, 19KT38, 19LT17, 20CT02, 20DT23, 20ET17, 20GT57, KME22A1989.
The recall notice does not specify a remedy or action steps beyond checking product details.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1964-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1964-2023 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.
