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Letter issued by FDA to increase awareness of potential risk associated with Medtronic NIM EMG Endotracheal Tube

Potential Risk of Airway Obstruction When Using Certain Electromyogram Endotracheal Tubes – Letter to Health Care Providers Today, the U.S. Food and Drug Administration (FDA) is issuing a Letter to Health Care Providers to increase awareness about the potential risk of airway obstruction when using silicone-based electromyogram (EMG) endotracheal tubes (Medtronic NIM Standard Reinforced EMG…

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Letter issued by FDA to increase awareness of potential risk associated with Medtronic NIM EMG Endotracheal Tube

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