Medtronic Xomed Recalls NIM TRIVANTAGE EMG Endotracheal Tube Due to Manufacturing Issue
Medtronic Xomed recalls specific NIM TRIVANTAGE EMG Endotracheal Tube models with certain product numbers and lots due to a manufacturing nonconformity that may cause multiple issues.
Recall notice
There is potential for multiple issues due to a manufacturing nonconformity.
Contact the company
What happened, in plain English
Medtronic Xomed is recalling specific models of NIM TRIVANTAGE EMG Endotracheal Tubes that have manufacturing defects. These tubes may cause multiple issues, but the recall does not specify what those issues are or if they pose a serious risk to users. Read more at govinfonow.com/recall/61406-medtronic-xomed-recalls-nim-trivantage-emg-endotracheal-tube-due-to.
Source Summary by GovInfoNow · govinfonow.com/recall/61406-medtronic-xomed-recalls-nim-trivantage-emg-endotracheal-tube-due-to · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0743-2022
Cite this page
“Medtronic Xomed Recalls NIM TRIVANTAGE EMG Endotracheal Tube Due to Manufacturing Issue.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61406-medtronic-xomed-recalls-nim-trivantage-emg-endotracheal-tube-due-to. Based on FDA recall #Z-0743-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0743-2022%22&limit=1).
Why it’s dangerous
The recall states there is potential for multiple issues due to a manufacturing nonconformity. However, the specific hazards and how they occur are not detailed in the record.
Who’s affected
Healthcare professionals and patients using the recalled endotracheal tubes may be affected. Those with the specific product numbers and lots listed are most at risk.
How to tell if you have this one
Check the product number and lot numbers listed in the recall. The affected tubes have specific product numbers (8229705-8229739) and corresponding lots as detailed in the recall.
- Brand
Medtronic Xomed- Product
NIM TRIVANTAGE EMG Endotracheal Tube- Category
Medical device
What to do — step by step
Check Product Details
Identify the product number and lot numbers from the list provided in the recall to determine if your tube is affected.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide distribution - US Nationwide and the countries of Algeria, Argentina, Australia, Austria, Bahrain, Bangladesh, Belgium, Brazil, Canada, Canary Islands, Chile, China, Colombia, Costa Rica, Croatia, Cyprus, Czech Republic, Denmark,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-0743-2022 (December 22, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0743-2022 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.