Teleflex recalls specific filter and catheter mounts for endotracheal tube connections due to incidents of device splitting or detaching during use. Affected units have unique identifiers listed in the recall notice.
Incidents of device splitting or detaching during use
Teleflex is recalling certain filter and catheter mounts used with endotracheal tubes because they can split or detach during use. This poses a risk of the device becoming dislodged, which could lead to breathing difficulties or other complications for patients.
The catheter mount can split or detach while in use, potentially causing the endotracheal tube to become dislodged from the patient. This could lead to breathing difficulties or other complications if the tube is no longer properly connected.
Healthcare professionals and patients using the recalled catheter mounts for endotracheal tube connections are most at risk. The specific units affected are those with the unique identifiers listed in the recall notice.
Check for the unique identifiers listed in the recall notice: (01)04026704561544(17)250728(10)KMH20H0092 and other similar codes. The product is sold only in the United States (OUS only).
Look for the unique identifiers listed in the recall notice to confirm if your device is affected.
The recall is due to incidents of the device splitting or detaching during use, which could lead to breathing difficulties or other complications.
Check the product identifiers listed in the recall notice to see if your device is affected. If it is, you should stop using it and contact Teleflex for further instructions.
The recall notice does not specify a fix or remedy for this issue.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-0077-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-0077-2023 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.
