Medtronic Xomed recalls NIM EMG Endotracheal Tubes with specific part numbers due to reported airway obstruction risks during use. Affected units include models REF 8229306-8229308.
The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.
Medtronic Xomed is recalling NIM EMG Endotracheal Tubes with part numbers REF 8229306, 8229307, and 8229308 because they have been reported to cause airway obstruction. This could lead to breathing difficulties or serious health issues for users.
The tubes have been reported to cause airway obstruction during medical procedures, which can lead to breathing difficulties. This risk is specific to the tube's design and usage in critical care environments.
Healthcare professionals using these tubes during medical procedures are most at risk, particularly those in critical care settings where airway management is essential.
Check for part numbers REF 8229306, 8229307, or 8229308 on the tube packaging or label. The Unique Device Identification (UDI) codes listed in the recall notice also help identify affected units.
Identify the part number on the tube to confirm if it matches REF 8229306, 8229307, or 8229308.
Part numbers REF 8229306, 8229307, and 8229308 are affected.
Check the part number on the tube or its packaging; affected units have part numbers REF 8229306, 8229307, or 8229308.
The recall notice does not specify a remedy, so affected users should check with Medtronic Xomed for further instructions.
We’ve drafted a message you can send Medtronic Xomed to request your refund or repair — edit it as you like.
Subject: Recall Z-1520-2022 — Medtronic Xomed Medtronic Xomed Hello, I own a Medtronic Xomed that is covered by recall Z-1520-2022 from Medtronic Xomed. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
