Teleflex recalls specific models of oral endotracheal tubes due to reports of 15mm connector disconnection. Affected units have unique batch numbers and reference codes. Consumers should check their product details to determine if they are impacted.
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 may 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 may become disconnected during use, potentially causing the tube to become dislodged from the patient's airway. This could lead to breathing difficulties or require immediate medical intervention.
Healthcare professionals and medical facilities using the affected endotracheal tubes are most at risk. Patients undergoing procedures with these tubes could face breathing issues if the connector disconnects.
Check for the product reference code REF 111781065 and batch numbers listed in the recall notice, such as 18FG20, 18FG31, or 19AG01. The tube has a Murphy Eye design with a high volume, low pressure cuff.
Look for the reference code REF 111781065 and batch numbers like 18FG20 or 19AG01 on the tube packaging or label.
Reach out to Teleflex directly for assistance with the recall process or to confirm if your specific tube is affected.
Teleflex is recalling these tubes after reports of the 15mm connector disconnecting from the tube, which could cause breathing difficulties during medical procedures.
Check for the reference code REF 111781065 and batch numbers listed in the recall, such as 18FG20, 18FG31, or 19AG01.
Contact Teleflex directly to determine if your tube is affected and follow their instructions for the recall process.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1955-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1955-2023 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.
