Teleflex recalls specific oral endotracheal tubes due to reports of 15mm connector disconnection. Affected models include batch numbers 18FG20 through 20FT64. Consumers should check their product details and contact Teleflex for guidance.
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 difficulties during medical procedures if the tube becomes disconnected.
The 15mm connector on the affected tubes can become disconnected during use. This disconnection could cause breathing problems for patients during medical procedures, especially if the tube is not properly secured.
Healthcare professionals and medical facilities using the recalled endotracheal tubes are most at risk. Patients undergoing procedures with these tubes may face breathing issues if the connector disconnects.
Check for the product name 'Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff' with the batch numbers listed in the recall notice. The specific reference number is REF 111781035.
Identify the batch numbers listed in the recall notice (e.g., 18FG20, 18FG31, etc.) to confirm if your tube is affected.
Reach out to Teleflex directly for further guidance on the recall and potential remedies.
Teleflex is recalling these tubes after reports of the 15mm connector disconnecting from the tube, which could cause breathing difficulties during medical procedures.
Check the batch numbers on your tube against the list provided in the recall notice (e.g., 18FG20, 18FG31, etc.).
Contact Teleflex directly for guidance on the recall and potential 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-1951-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1951-2023 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.
