Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected models include batch numbers 19ET51 through KME22H1360. Consumers should check their tube's batch number and 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 from the tube. This could lead to breathing issues during medical procedures if the tube becomes disconnected.
The 15mm connector on the affected tubes has been reported to disconnect during use. This disconnection could cause breathing difficulties or require immediate medical intervention if the tube becomes separated from the patient.
Healthcare professionals and patients using these endotracheal tubes during medical procedures. Those with the specific batch numbers listed are most at risk.
Check the batch number on the tube's packaging or label. Affected products include batch numbers 19ET51, 19FT29, 19GT05, 19GT35, 19HT79, 19JT51, 19KT06, 19LT28, 20AT05, 20AT37, 20AT54, 20BG15, 20DT24, 20ET03, KME21B0529, KME21C0887, KME21D0327, KME21F0137, KME21K0799, KME21K0800, KME22A2704, KME22C0981, KME22C1568, KME22D0029, KME22H0686, KME22H1360.
Look for the batch number on the tube's packaging or label to determine if it's affected.
Reach out to Teleflex for further instructions on how to handle the affected tubes.
Teleflex is recalling specific endotracheal tubes due to reports of the 15mm connector disconnecting from the tube during use.
Check the batch number on the tube's packaging or label. Affected products include batch numbers 19ET51 through KME22H1360.
Contact Teleflex for instructions on how to handle the affected tubes. The remedy is not specified 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-1925-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1925-2023 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.
