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Do Not Use Medtronic NIM Contact and Standard EMG Endotracheal Tubes - Letter to Health Care Providers
Today, the U.S. Food and Drug Administration (FDA) issued a Letter to Health Care Providers to alert providers and facilities to stop using NIM Contact EMG Reinforced Endotracheal Tubes and NIM (Standard) EMG Reinforced Endotracheal Tubes by Medtronic and to help ensure awareness of the manufacturer’s recall notice and recommended actions.
The Letter to Health Care Providers includes important information about this issue including:
- Recommendations for health care providers and facilities.
- The FDA’s actions to address the issue.
- Instructions for reporting problems to the FDA.
Questions?
If you have questions about this letter to health care providers, contact the Division of Industry and Consumer Education (DICE).
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