Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected models include REF 112082075 with listed batch numbers. 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 that have reported issues with the 15mm connector coming loose. This could lead to disconnection during medical procedures, potentially causing complications for patients.
The 15mm connector on the affected tubes has been reported to disconnect, which could lead to the tube becoming dislodged from the patient's airway. This might cause breathing difficulties or other medical complications during procedures.
Healthcare professionals and medical facilities using the recalled endotracheal tubes are most at risk. Patients receiving these tubes during procedures may face complications if the connector disconnects.
Check for the product reference number REF 112082075 and batch numbers listed in the record (e.g., 18FG29, 18GG13, etc.). The tubes have a specific UDI/DI code 14026704341433.
Look for the product reference number REF 112082075 and batch numbers listed in the recall notice to confirm if your tube is affected.
Teleflex reports that the 15mm connector on these tubes has disconnected, which could lead to the tube becoming dislodged during medical procedures.
Check for the product reference number REF 112082075 and batch numbers listed in the recall notice (e.g., 18FG29, 18GG13, etc.).
The recall does not specify a remedy, so contact Teleflex directly for guidance on next steps.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1889-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1889-2023 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.
