Teleflex recalls specific models of oral endotracheal tubes due to reports of 15mm connector disconnection. Affected units have batch numbers listed in the recall notice.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling certain oral endotracheal tubes because reports indicate the 15mm connector can disconnect from the tube. This could lead to breathing issues during medical procedures if the tube becomes disconnected.
The 15mm connector on these tubes has been reported to disconnect, which could cause the tube to become unplugged from the patient's airway. This might lead to breathing difficulties or the need for emergency reconnection during medical procedures.
Healthcare professionals using these tubes during medical procedures are most at risk. Patients receiving anesthesia or critical care may be affected if the tube disconnects during surgery.
Check the product's batch numbers listed in the recall notice: 18FT35, 18FT39, 18GG17, 18GG18, 18GT32, and others. The product name is Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff.
Inspect the 15mm connector on the tube for signs of disconnection or damage.
The recalled tubes are Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff with batch numbers listed in the recall notice.
Check the batch numbers on your tube: 18FT35, 18FT39, 18GG17, 18GG18, 18GT32, and others as listed in the recall notice.
The recall does not require immediate discontinuation; healthcare professionals should check for disconnection before use.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1953-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1953-2023 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.
