Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected models include Magill with batch numbers 19ET31 through 20GT37. 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 that have reported disconnections at the 15mm connector. This could lead to breathing issues during medical procedures if the tube becomes disconnected.
The 15mm connector on the endotracheal tube can disconnect during medical procedures. This disconnection could interrupt the patient's breathing and cause serious health issues if not addressed immediately.
Healthcare professionals and medical facilities using the recalled endotracheal tubes are most at risk. Patients receiving these tubes during procedures may face breathing complications if disconnection occurs.
Check the batch number on the tube's packaging or label. Affected tubes have batch numbers starting with 19ET31 through 20GT37. The product is identified as a Magill endotracheal tube.
Look for batch numbers on the tube's packaging or label, which range from 19ET31 to 20GT37.
Reach out to Teleflex for further assistance or to confirm if your tube is affected.
Teleflex reports disconnections of the 15mm connector on these endotracheal tubes, which could interrupt breathing during medical procedures.
Check the batch number on the tube's packaging or label. Affected tubes have batch numbers starting with 19ET31 through 20GT37.
Contact Teleflex directly to determine if your tube is affected and to get 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-1926-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1926-2023 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.
