Teleflex Endotracheal Tubes Recall: Risk of Connector Disconnection

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Recalling firmTELEFLEX LLC3015 Carrington Mill Blvd, N/A · Morrisville, NC 27560-5437

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Teleflex is recalling certain endotracheal tubes because reports show the 15mm connector can disconnect from the tube. This could lead to breathing issues during medical procedures if the tube becomes disconnected.

Why it’s dangerous

The 15mm connector on the endotracheal tube can become disconnected during use, which may cause breathing difficulties. This disconnection could lead to serious complications if the tube is no longer properly connected to the patient's airway.

Who’s affected

Healthcare professionals using the affected endotracheal tubes for medical procedures are most at risk. Patients receiving these tubes during surgery or critical care may also be affected.

How to tell if you have this one

Check for the model name 'Magill' and batch numbers listed: 19ET11, 19GT51, 19JT20, 20AT13, KME20H2315, KME21A2778, KME22A0155, KME22A2335, KME22E0288, KME22E1272, KME22F1551.

Brand
Teleflex
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for the batch numbers listed: 19ET11, 19GT51, 19JT20, 20AT13, KME20H2315, KME21A2778, KME22A0155, KME22A2335, KME22E0288, KME22E1272, KME22F1551.

✎ GovInfoNow

Questions people ask

Why is this recall happening?

Teleflex is recalling these endotracheal tubes after reports of the 15mm connector disconnecting from the tube during use.

What should I do if I have this tube?

Check the batch numbers on the tube to see if it's affected. If it is, contact Teleflex for further instructions.

Is there a risk of serious injury?

Yes, disconnection could cause breathing issues during medical procedures, which may lead to serious complications.

Take action

Contact Teleflex

We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1931-2023 — Teleflex Teleflex

Hello,

I own a Teleflex that is covered by recall Z-1931-2023 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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Where this comes from

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.

Official source: FDA Recall #Z-1931-2023 (May 25, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1931-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

TELEFLEX LLC recalls Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380055

Use caution until it’s fixed