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.
There is potential for multiple issues due to a manufacturing nonconformity.
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.
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.
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.
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.
Identify the product number and lot numbers from the list provided in the recall to determine if your tube is affected.
The recall states there is potential for multiple issues due to a manufacturing nonconformity, but the specific hazards are not detailed in the record.
The recall does not specify a remedy or immediate action, so there is no instruction to stop using them now.
Check the product number and lot numbers listed in the recall details to see if your tube matches the affected models.
We’ve drafted a message you can send Medtronic Xomed to request your refund or repair — edit it as you like.
Subject: Recall Z-0743-2022 — Medtronic Xomed Medtronic Xomed Hello, I own a Medtronic Xomed that is covered by recall Z-0743-2022 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.
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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.
