Teleflex recalls specific endotracheal tubes due to reports of 15mm connector disconnection. Affected products include certain batch numbers and reference codes. Consumers should check their items 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 endotracheal tubes with a specific connector design that has reportedly disconnected. This could lead to breathing issues during medical procedures if the tube becomes disconnected. Affected units have unique batch numbers and reference codes.
The 15mm connector on the affected tubes has reportedly come loose during use. This disconnection could interrupt the tube's connection to the patient's airway, potentially causing breathing difficulties or requiring emergency intervention during medical procedures.
Healthcare professionals using these endotracheal tubes in medical settings are most at risk. Patients receiving procedures with the affected tubes could face breathing complications if disconnection occurs.
Check for the reference code 112082065 and batch numbers listed in the recall notice, such as 18FG23 through KME22H2054. These specific batch numbers and reference codes identify the affected products.
Identify the reference code and batch numbers listed in the recall notice to confirm if your tube is affected.
Teleflex reports that the 15mm connector on these endotracheal tubes has disconnected during use, potentially causing breathing issues.
Check for the reference code 112082065 and batch numbers listed in the recall notice, such as 18FG23 through KME22H2054.
Contact Teleflex directly to confirm if your tube is affected and follow their instructions for next steps.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-1887-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-1887-2023 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.
