Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected models include Magill with batch numbers 18FG31 through KME22D1803. Contact Teleflex for details.
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Teleflex is recalling certain endotracheal tubes because reports indicate the 15mm connector can disconnect. This could lead to breathing issues during medical procedures if the tube becomes disconnected.
The 15mm connector on these endotracheal tubes has been reported to disconnect, potentially causing breathing difficulties. This disconnection could occur during medical procedures if the tube is moved or handled improperly.
Healthcare professionals using these tubes during medical procedures are most at risk. Patients receiving endotracheal tube care may also be affected if the tube disconnects.
Check for the product name 'Endotracheal Tube oral/nasal uncuffed/plain - Magill' with batch numbers listed: 18FG31, 19BT11, 19ET72, 19JT30, 20AT13, 20BT13, 20DT13, KME21D0600, KME21J0790, KME22A0448, KME22D1803.
Identify the batch numbers on the tube to confirm if it is affected.
Reach out to Teleflex for further instructions on handling the recalled tubes.
Teleflex is recalling these tubes after reports of the 15mm connector disconnecting, which could cause breathing issues during medical procedures.
Check for the batch numbers listed: 18FG31, 19BT11, 19ET72, 19JT30, 20AT13, 20BT13, 20DT13, KME21D0600, KME21J0790, KME22A0448, KME22D1803.
Contact Teleflex for specific instructions on handling the recalled tubes.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1932-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1932-2023 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.
