Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected models include REF 100380050 with batch numbers listed. Stop using if you own these items.
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 show 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 endotracheal tubes has been reported to disconnect from the tube itself. This disconnection could interrupt the patient's breathing during medical procedures, potentially causing serious health risks.
Healthcare professionals and patients using these endotracheal tubes during medical procedures are most at risk. The affected products are used in critical care settings where disconnection could cause breathing problems.
Check for the product name 'Endotracheal Tube oral/nasal uncuffed/plain - Magill' with reference number REF 100380050. The batch numbers listed include 18FG05 through 20DT13 and other codes like KME20H2359.
Look for the reference number REF 100380050 and batch numbers listed in the recall notice.
Reports of the 15mm connector disconnecting from the endotracheal tube have been identified as the hazard.
The recall does not specify a remedy, so contact Teleflex directly for guidance on next steps.
Yes, the affected batch numbers include 18FG05, 18FT26, 18GT27, and others listed in the recall notice.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1930-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1930-2023 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.
