Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected models include REF 112082090 with certain batch numbers. 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 specific endotracheal tubes that have reported issues with the 15mm connector disconnecting. This could lead to breathing difficulties during medical procedures if the tube becomes disconnected.
The 15mm connector on the affected endotracheal tubes can become disconnected during use, potentially causing breathing difficulties for patients. This disconnection risk occurs during medical procedures where the tube is in place.
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 the connector disconnects.
Check for the product reference number REF 112082090 and batch numbers listed in the recall notice. The affected tubes have specific batch codes such as 18FG23, 18FT17, and others listed in the recall details.
Identify if your endotracheal tube has the reference number REF 112082090 and one of the listed batch numbers.
Teleflex is recalling these tubes due to reports of the 15mm connector disconnecting, which could cause breathing difficulties during medical procedures.
Check if your tube has the reference number REF 112082090 and one of the listed batch numbers. If it does, contact Teleflex for further instructions.
The recall reports disconnection issues that could lead to breathing difficulties, but the remedy does not specify a stop-use action, so the risk level is use caution.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1892-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1892-2023 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.
