Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected products include certain batch numbers and model references.
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 coming loose. This could lead to medical complications during use if the tube disconnects.
The 15mm connector on the endotracheal tube can become disconnected during use, potentially causing the tube to become dislodged from the patient's airway. This could lead to breathing difficulties or other medical complications if not addressed immediately.
Healthcare professionals using these endotracheal tubes in medical settings are most at risk. Patients receiving care with the affected tubes may experience complications if the connector disconnects.
Check for the product name 'Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff' with the reference number 112082080. Affected units include specific batch numbers listed in the recall notice.
Look for the reference number 112082080 and batch numbers listed in the recall notice to confirm if your tube is affected.
Teleflex reports that the 15mm connector on these endotracheal tubes may disconnect, which could lead to medical complications if the tube becomes dislodged.
Check for the reference number 112082080 and batch numbers listed in the recall notice. Affected products include specific batch numbers such as 18GG11, 18GG12, and others.
The recall notice 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-1890-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1890-2023 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.
