Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected models include batch numbers 18KG25 through KME22F2582. Consumers should check their tube's batch number 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 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 these endotracheal tubes can become disconnected during use, potentially causing breathing difficulties. This disconnection risk is specific to the affected batch numbers and models.
Healthcare professionals and patients using endotracheal tubes during medical procedures are most at risk. The affected tubes are used in critical care settings where disconnection could cause breathing issues.
Check the batch number on the tube's packaging or label. Affected products include batch numbers 18KG25, 19BT19, 19CT22, 19CT39, 19ET06, KME21L2054, KME22A2341, KME22C2640, KME22E2541, KME22F1554, and KME22F2582.
Look for the batch number on the tube's packaging or label to confirm if it is affected.
Reach out to Teleflex directly for further instructions on how to handle the affected tubes.
Reports indicate the 15mm connector can disconnect from the tube, potentially causing breathing difficulties during medical procedures.
Check the batch number on the tube's packaging or label. Affected products include batch numbers 18KG25, 19BT19, 19CT22, 19CT39, 19ET06, KME21L2054, KME22A2341, KME22C2640, KME22E2541, KME22F1554, and KME22F2582.
The recall does not require immediate discontinuation; healthcare professionals should check the batch number and contact Teleflex for further instructions.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1939-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1939-2023 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.
